Haplotype i

Human Y-chromosome DNA haplogroup - Wikipedia

Haplogroup I-M170 - Wikipedi

A haplotype is defined as the combination of alleles for different polymorphisms that occur on the same chromosome (189), and for any given stretch of chromosomal DNA an individual will have two haplotypes, although at a population level there may be numerous haplotypes for any given stretch of chromosomal DNA Haplotype. A haplotype is defined as the combination of alleles for different polymorphisms that occur on the same chromosome (189), and for any given stretch of chromosomal DNA an individual will have two haplotypes, although at a population level there may be numerous haplotypes for any given stretch of chromosomal DNA Haplotype. Binnen de genetica is een haplotype de combinatie van allelen zoals die voorkomen op een uniek chromosoom. Het kan gebruikt worden voor de basevolgorde van een stuk van een bepaald chromosoom, of voor een verzameling allelen zoals die samen voorkomen. == Uitleg == De lichaamscellen van mensen en zoogdieren zijn diploïd: ze hebben 2. mtDNA Haplogroup I * * * * * * * * * * * * * * * * * * * * Descendants of 'Iris' Hello! We welcome everyone with mtDNA test results in the Family Tree DNA system, confirming that they belong to Haplogroup I. Ha p logroup I i s a West Eurasian haplogroup. It is relatively rare and one of the older mtDNA haplogroups in Europe

Haplogroepen zijn groepen individuen die geclassificeerd worden aan de hand van het haploïde DNA. Haplogroepen worden weer ingedeeld in familiaire haplotypes. Deze classificatie is van belang voor genografie, een wetenschappelijke tak die zich bezighoudt met hoe een organisme zich in de prehistorie heeft ontwikkeld en verspreid Wat is de betekenis van Haplotype? Op Ensie, Encyclopedie sinds 1946, vind je 1 betekenis van het woord Haplotype. Door experts geschreven Haplotype Binnen de genetica is een haplotype de combinatie van allelen zoals die voorkomen op een uniek chromosoom. Het kan gebruikt worden voor de basevolgorde van een stuk van een bepaald chromosoom, of voor [.. Mouse Haplotype Table MHC Class I MHC Class II MHC Class Ib Mouse Strains MHC Haplotype H-2K H-2D H-2L I-A I-E Qa-2 Qa-1 CD45 (Ly-5) Thy-1 (CD90) NK1.1 101/- k k k null k k 129/- b b b null b null a b 2 2 - A/J a k d d k k a a 2 2 - A/2G a k d d k k AKR/J k k k null k k b b 2 1 - AL/N a k d d k k a AU/SsJ q q q q q null - BaLB/cAnN d d d d d d. Haplotype er en kombinasjon av alternative gener (alleler) som ligger nær hverandre på kromosomet. Disse nedarves under ett fra en av foreldrene. Fordi arvestoffet DNA viser så stor variasjon (se SNP-er og STR-er under human genetikk og human genomprosjektet), vil en haplotype av en viss lengde være nærmest individspesifikt på grunn av overkrysninger mellom de to haplotypene i hvert.

Haplotype - Wikipedi

Haplotype (HT) Haplotype (HT) - /hap•lo•type/ - A set of numbers or letters obtained from the DNA test of an individual. A set of alleles for genetic markers (a set of gene or genetic marker DNA sequences) inherited as a unit If you find our videos helpful you can support us by buying something from amazon.https://www.amazon.com/?tag=wiki-audio-20Haplotype=====Image-Copyright-In..

A haplotype (Greek haploos = simple) is the genetic constitution of an individual chromosome. Haplotype may refer to only one locus or to an entire genome. In the case of diploid organisms such as humans, a genome-wide haplotype comprises one member of the pair of alleles for each locus (that is, half of a diploid genome). An organism's haplotype is studied using a genealogical DNA test. The. Haplotype-phenotype association mapping Using the two-layer model, we can define and infer local haplotype sharing (LHS) between cohort individuals. Then we may link phenotypes and the LHS at each marker to perform association mapping. Because LHS is inferred using local haplotypes, our method detects (unspecified) haplotype association haplotype. [ hap´lo-tīp] 1. a set of alleles of a group of closely linked genes, such as the HLA complex, which are usually inherited as a unit, an individual inheriting a complete haplotype from each parent. 2. the genetic constitution of an individual at a set of linked genes Haplotype definition is - a group of alleles of different genes (as of the major histocompatibility complex) on a single chromosome that are closely enough linked to be inherited usually as a unit Een haplotype omvat meerdere genen die samen met eventuele niet-coderende segmenten gekoppeld overerven. Dat betekent dat steeds dezelfde combinaties van allelen bij elkaar blijven en dat er binnen een haplotype een grote afwijking van koppelingsevenwicht is. Het meest bekende voorbeeld van een haplotype is het mitochondriaal genoom (mtDNA)

Haplotyp (z gr. ἁπλοῦς, haploûs − prosty, pojedynczy) − pojęcie w genetyce, oznaczające grupę genów, którą organizm odziedziczył po jednym z rodziców. Innymi słowy, jest to zestaw polimorfizmów pojedynczych nukleotydów (SNP), położonych na jednej chromatydzie, który dziedziczy się jako zestaw sprzężonych ze sobą alleli Sometimes we've been doing genetic genealogy for so long we forget what it's like to be new. I'm reminded, sometimes humorously, by some of the questions I receive. When I do DNA Reports for clients, each person receives a form to complete with a few questions designed to give them the opportunity to tell me wha Haplotype en Biologie van A tot Z · Bekijk meer » Erysiphe necator. Erysiphe necator (syn. Uncinula necator) (teleomorfe fase) is een obligate, biotrofe, echte meeldauw schimmel, die druiven aantast en behoort tot de orde Erysiphales van de ascomyceten. Nieuw!!: Haplotype en Erysiphe necator · Bekijk meer » Genetische associati 0:00 Introduction02:28 Mendel's First Law02:56 Mendel's Second Law04:43 Using lines to represent haplotype frequencies05:28 The 1:1:1:1 ratio05:40 Conclusio

HLA-DQB1 - Wikipedia

En haplotype er en kombinasjon av alleler på nærliggende loci i et DNA-molekyl.En haplotype kan omfatte et vilkårlig antall loci, fra kun noen få loci, til et helt kromosom.En haplotype går gjerne i arv hvis det ikke forekommer en rekombinasjon.. Haplotype må ikke forveksles med genotype.En organismes haplotype i et kromosom følger ikke automatisk av organismens genotype Here we show that APOBEC3H haplotype I (A3H-I) provides a likely solution to this paradox. A3B-null tumours with this mutational bias have at least one copy of A3H-I despite little genetic linkage between these genes. Although deemed inactive previously,. if that haplotype is concentrated in a certain geographic area, it may indicate a glacial refugium or point of invasion. This would depend on the scale of your sampling, mobility of organism, etc

Because obtaining haplotype information directly from experiments can be cost prohibitive in most studies, especially in large scale studies, haplotype analysis presents many unique challenges. In this chapter, we focus on two main issues: haplotype inference and haplotype-association analysis Haplotype is defined as one person's set of values for the DYS markers that have been tested. In other words, your yDNA test results. Think of Haplotypes as leaves on a tree, and a Haplogroup as a limb of that tree. Haplotype is a contaction of the phrase haploid genotype A collection of genealogical profiles related to I2-M223 (Y-DNA) This project is for people who have tested and been assigned the paternal haplogroup I2a2a (M223) and also for people who are believed to have belonged to this paternal haplogroup based on tests done on descendants.. Formerly: I2b1 (2008) Defining Mutation

Haplotype - Genome.go

De term karyotype wordt daarnaast ook gebruikt voor de zeer kort opgeschreven formule die beschrijft hoe bij een bepaald individu het karyogram eruitzag. De formule drukt het aantal chromosomen uit en kan ook eventuele afwijkingen weergeven. Bij mensen zijn de normale karyogrammen [46, XX] voor een vrouw en [46, XY] voor een man Defining haplotype blocks. To define haplotypes, we first generated whole-chromosome pairwise alignments between all 15 cultivars using NUCmer, excluding pairwise comparisons between scaffold. We present a novel pipeline and methodology for simultaneously estimating isoform expression and allelic imbalance in diploid organisms using RNA-seq data. We achieve this by modeling the expression of haplotype-specific isoforms. If unknown, the two parental isoform sequences can be individually reconstructed. A new statistical method, MMSEQ, deconvolves the mapping of reads to multiple.

Haplotype discovery can be made within single reads or span paired reads, and can leverage long read technology by targeting any length of haplotype. Haplotype-based genotyping is applicable in all allopolyploid genomes and provides confidence in marker identification and in silico-based genotyping for polyploid genomics Haplotype frequency distributions among hosts revealed nonrandom laying in both cowbird species. In shiny cowbirds, we found differences in the distribution of haplotypes between house wrens and the other three hosts (rufous-collared sparrows, brown-and-yellow marshbirds, and chalk-browed mockingbirds; pairwise Φ ST values = 0.20-0.23, P < 0.001)

You inherit one haplotype from each parent. Therefore, there are a total of four different haplotype combinations from 2 parents.. There is a basic rule in HLA inheritance. The rule is: you have a 25% chance of inheriting all of the same HLA (same 2 haplotypes) as any one of your siblings, you have a 25% chance of not inheriting any of the same HLA (none of the same haplotypes) and you have a. 1 Induced mutagenesis by the DNA cytosine deaminase APOBEC3H Haplotype I protects against lung cancer Mark A. Hix1,#, Lai Wong2,#, Ben Flath2, Linda Chelico2,*, G. Andrés Cisneros1,3,* 1. Haplotypes and Understanding Haplotype Networks. Okay so lamarckwaswrong asked me to help out with an issue regarding the interpretation of haplotype networks. I thought this might be a bit of a general interest query, so I decided to make a more complete post about what they are, how they work, and how to interpret them

Haplotype - ISOGG Wik

haplotype - (genetics) a combination of alleles (for different genes) that are located closely together on the same chromosome and that tend to be inherited together. genetic science, genetics - the branch of biology that studies heredity and variation in organisms Haplotype analysis of 120 cloned key genes associated with major grain yield and quality related traits in rice. The chosen 120 genes were previously functionally characterized and were reported to govern/regulate several major grain yield (87 genes) and quality related traits (33 genes) such as tiller number, flowering, panicle architecture, lodging resistance, single plant yield, grain.

The germline JAK2 haplotype known as GGCC or 46/1 haplotype (haplotype GGCC_46/1) consists of a combination of single nucleotide polymorphisms (SNPs) mapping in a region of about 250 kb, extending from the JAK2 intron 10 to the Insulin-like 4 (INLS4) gene.Four main SNPs (rs3780367, rs10974944, rs12343867, and rs1159782) generating a GGCC combination are more frequently indicated to. haplotype groups, and the remaining haplotypes were classified as rare and excluded from further analysis. Genotypes that could not be characterized because of missing data were grouped as missing and were omitted from further analysis. The initial SNP haplotype characterization identified six haplotype groups (Hap1-Hap6), which accounted fo A collection of genealogical profiles related to I1-M253 (Y-DNA) Var lensmann i Gand fra 1641. Han var leilending på Skei, men eide mye jord andre steder og var en av de rikeste bøndene på Jæren på den tiden selscan is a tool for haplotype-based scans to detect natural selection, which are useful to identify recent or ongoing positive selection in genomes. It is an efficient multithreaded application that implements Extended Haplotype Homozygosity (EHH), Integrated Haplotype Score (iHS), and Cross-population EHH (XPEHH) Hello everyone! I'm a beginner in bioinformatics, but I would like to know which program (s) I should use to building a haplotype family using vcf files and if there is some good program to visualize the results

TNF2 has previously been shown to be associated with the MHC haplotype HLA A1-B8-DR3-DQ2, which confers susceptibility to CD. We have analyzed the distribution of TNF2 alleles in a group of celiac patients (n = 52) compared to controls (n = 52) in an effort to evaluate its role, if any, in susceptibility to the condition We untangled key regions of the genetic architecture of grain yield (GY) in CIMMYT spring bread wheat by conducting a haplotype-based, genome-wide association study (GWAS), together with an investigation of epistatic interactions using seven large sets of elite yield trials (EYTs) consisting of a total of 6,461 advanced breeding lines. These lines were phenotyped under irrigated and stress.

Haplotype - SNPedi

  1. Several authors have proposed haplotype motifs based on site variants at the mitochondrial genome (mtDNA) and the non-recombining portion of the Y chromosome (NRY) to trace the genealogies of Jewish people. Here, we analyzed their main approaches and test the feasibility of adopting motifs as ancestry markers through construction of a large database of mtDNA and NRY haplotypes from public.
  2. Review and cite HAPLOTYPE ANALYSIS protocol, troubleshooting and other methodology information | Contact experts in HAPLOTYPE ANALYSIS to get answer
  3. Generating chromosome-level, haplotype-resolved assemblies of heterozygous genomes remains challenging. To address this, we developed gamete binning, a method based on single-cell sequencing of haploid gametes enabling separation of the whole-genome sequencing reads into haplotype-specific reads sets. After assembling the reads of each haplotype, the contigs are scaffolded to chromosome level.
  4. A haplotype approach may (i) overcome the inherent biallelic limitation of SNP markers and accurately capture the allelic diversity of the causal genes present in a collection of accessions; (ii) optimize the use of high‐density marker data, including linkage within a locus, the evolutionary history of markers, and the pattern of inheritance.

Haplotypes - an overview ScienceDirect Topic

  1. ently, MS. DR15 has been investigated as a genetic risk factor for MS in case-control and family-based studies from countries around the world
  2. Mouse sperm carrying a genetic sequence called the t-haplotype will poison their competitors, then make an 'antidote' only for themselves, new research finds
  3. A Practical Haplotype Graph can be used for many types of data processing and analysis. You can build a PHG from genome assembly-quality genomes or whole-genome resequencing data and use it to impute either variants or haplotypes, both for taxa within the database and for new taxa that are not included in the DB
  4. HapCUT2: robust and accurate haplotype assembly for diverse sequencing technologies About: HapCUT2 is a maximum-likelihood-based tool for assembling haplotypes from DNA sequence reads, designed to just work with excellent speed and accuracy

Video: Haplotype - an overview ScienceDirect Topic

For phased haplotype data for a single chromosome as a VCF file of N individuals and M SNPs, we can simply generate a 2N x M haplotype matrix using scikit-allel. python generateNPYfromVCF.py -vcf chr1.vcf.gz -out chr1 # Saves int8 NumPy matrix in binary format (chr1.npy 1 Lecture 3: Haplotype reconstruction Su‐In Lee, CSE & GS, UW suinlee@uw.edu Statistical Genetics -Part I 1 Outline Basic concepts Allele, allele frequencies, genotype frequencies Haplotype, haplotype frequency Recombination rate Linkage disequilibrium Haplotype reconstruction Parsimony‐based approach EM‐based approac an haplotype. I would like to contibute to bioperl these two modules. Bio::Haplotype::Select Bio::Haplotype::Tag I also have stand alone examples about how the code is working and about what to input and what you get from the module

Haplotype - definitie - Encycl

  1. Rijmwoordenboek HAPLOTYPE 92 rijmwoorden in Van Dale Rijmwoordenboek. Rijmen op HAPLOTYPE. Wat rijmt er op HAPLOTYPE
  2. Segmented HAPlotype Estimation and Imputation Tools version 4 (SHAPEIT4) SHAPEIT4 is a fast and accurate method for estimation of haplotypes (aka phasing) for SNP array and sequencing data. The version 4 is a refactored and improved version of the SHAPEIT algorithm with multiple key additional features
  3. A modal haplotype for all of I1 would not be meaningful because the different varieties of I1 have not shared a common ancestor for thousands of years, but key markers do unify the subclade (highlighted in red in the tables). Among European haplotypes, DYS455=8 is virtually exclusive to I1
  4. ary sample of unrelated subjects with an example from the Multiethnic Cohort Study. Hum Hered 55(1.
  5. The t-haplotype alleles play dirty when it comes to reaching the egg first. In order for their nefarious scene to work, just the right amount of a certain protein has to be present
  6. So a haplotype may, for example, be named KH-001A or KH-022B. To supplement the haplotype name and provide further information, it was suggested that following the haplotype designation a 17-digit binary code would indicate the presence or absence of the genes on the haplotype
  7. Haplotype Map These ancestral genomic segments are inherited as discrete units with little genetic shuffling across generations. Because haplotypes are shared by a majority of the human population, they can be used to decipher the genetic differences that make some people more susceptible to disease than others

Haplotype frequency estimation and reconstruction, flexible in missing data patterns and X chromosome data, haplotype-specific tests: Limited to about 15 SNPs and slow with multiple multiallelic loci with missing data: HAP: hap,mia: hap.txt: Large number of SNPs and multiple imputations, missing data, multiallelic loci: Possibly sub-optimal. As nouns the difference between haplotype and genotype is that haplotype is (genetics) a group of alleles that are transmitted together while genotype is (genetics) the combination of alleles, situated on corresponding chromosomes, that determines a specific trait of an individual, such as aa or aa Pr(case haplotype data) Pr(control haplotype data) Pr(case and control haplotype data combined) where the denominator represents the probability of the haplotype data computed under the null hypothesis that they came from a single homogenous group, and the numerator represents the probability of the haplotype data under the alternative hypothesis that the case and control groups differ A new statistical method for haplotype reconstruction from population data. American Journal of Human Genetics, 68, 978--989. [2] Stephens, M., and Donnelly, P. (2003). A comparison of Bayesian methods for haplotype reconstruction from population genotype data. American Journal of Human Genetics, 73:1162-1169. [3] Stephens, M., and Scheet, P.

I Haplogroup mtDNA - Background FamilyTreeDN

Goal The Haplotype Reference Consortium (HRC) will create a large reference panel of human haplotypes by combining together sequencing data from multiple cohorts. Uses The reference panel will be used for genotype imputation and phasing in other cohorts, typically genome-wide association studies (GWAS) , where genotypes are available from genome-wide SNP microarrays Y-STR Haplotype Reference Database (YHRD) is a searchable worldwide database of Y-STR Haplotypes in various formats along with tools build upon their distribution Resolving genomes at haplotype level is crucial for understanding the evolutionary history of polyploid species and for designing advanced breeding strategies. Polyploid phasing still presents considerable challenges, especially in regions of collapsing haplotypes.We present WhatsHap polyphase, a novel two-stage approach that addresses these challenges by (i) clustering reads and (ii. Bekijk hier de voortgangsrapportage 2014 van Haplotype Atlas of Potato. VOORTGANG 2015 Bekijk hier de voortgangsrapportage 2015 van Haplotype Atlas of Potato. VOORTGANG 2016 Bekijk hier de voortgangsrapportage 2016 van Haplotype Atlas of Potato. EINDRAPPORTAGE Bekijk hier de eindrapportage van Haplotype Atlas of Potato

Achondroplasia with the FGFR3 1138g→a (G380R) mutation inMaternal Haplogroup Chart RF Finder Matches | These are

Haplogroep - Wikipedi

This mutation occurs in the motif 73-3010-16162, which defines H1a. The finding of an Eastern Slav individual bearing haplotype 73-16093-16162 and lacking H1 defining transition at np 3010 hints that motif 73-16162 may have arisen, though rarely, more than once in haplogroup H (fig. 2A) Supported formats: 23andMe raw data, deCODEme raw data, Differences to rCRS (mutation list), FASTA, GenBank Flat File Format, ASN1 Help: Frequently Asked Questions; Frequently Asked Questions for Advanced Options; Directions for 23andMe customers; Directions for deCODEme customer His mother is Beatrice Call 1916-1989 and her prior husband was Edward Anderson who we believe is not the father of Wallace. Beatrice Call's parents were John Call (1876-1941) and Harriet Amelia Jones (1892-1968) and she was listed as adopted on her marriage certificate. My paternal half brother did 23&me and his y paternal haplotype is R-CTS241 I can build a haplotype net with the following script: x <- read.dna(file=x.fas,format=fasta) h <- haplotype(x) net <- haploNet(h) plot(net) I'd like to set in the dnabin data the label of the original population of each taxa, so i could have piecharts of different colors (of haplotypes from different populations) in the resulting network Haplotype tests now are used routinely to identify new recessive disorders and to track the carrier status of genotyped animals. Changes in the reporting of recessive factors that affect fertility and stillbirth recently have been described in detail ( VanRaden et al., 2013). Carrier status for Holstein haplotypes with mutations for bovine.

haplotype. haplotype: translation. n. a complete set of HLA antigens inherited from either parent. The new mediacal dictionary. 2014. haploid; happy puppet syndrome; Look at other dictionaries haplotype: in een strikte betekenis, de specifieke allelen van verschillende loci die zich op dezelfde fysische chromosoom bevinden. In de brede betekenis zeggen we dat een set allelen voor verschillende loci een haplotype vormen. We erven dan een haplotype van onze moeder en een haplotype van onze vader The word is in the Wiktionary 3 short excerpts of Wiktionnary (A collaborative project to produce a free-content dictionary.) — English words — haplotype n. (genetics) A group of alleles that are transmitted together. haplotype v. (genetics) To characterize with respect to haplotype The rare haplotypes are combined to form the baseline haplotype in the logistic regression model. From the Cambridge English Corpus Observed haplotype diversity and number of haplotypes for the smallest study fragment (120 ha) were 0.556 and 3 haplotypes, respectively

For what they were

Developing a Haplotype Map of the Human Genome for Finding Genes Related to Health and Disease Washington, D.C. July 18-19, 2001 Introduction. So far about 2.4 million DNA sequence variants (single nucleotide polymorphisms or SNPs) have been discovered in the human genome, and millions more exist Haplotype analysis is designed for molecular genetic testing in order to identify DNA segments that share similarities. Haploview has been created to improve the tasks relating to such analysis Haplotype testing in PLINK requires that the user supplies a file listing the haplotypes to be tested (Some precomputed lists are given below which might be useful in some circumstances.) The formats of these files are described below. An alternative is to specify a simple,. Merlin has three haplotype estimation modes. It can either provide haplotypes corresponding to the most likely pattern of gene flow (--best command line option), sample gene flow patterns according to their likelihood (--sample) or provide all non-recombinant haplotypes (--zero --all). For this example, we will use the first option Moved Permanently. The document has moved here

The original haplotype map file format. It has a header and a body as shown below. The header is a standard SAM header, with an @HD line to define the file type and @SQ lines to define the reference contigs. You can easily derive such a header from your reference dictionary file haplotipas statusas T sritis augalininkystė apibrėžtis Artimai susijusių vienos chromosomos alelinių genų derinys; kartais DNR sekos nukleotidų derinys. atitikmenys: angl. haplotype rus. гаплоти Fifteen breeds were characterized by a single Y chromosome haplotype. Breed-specific haplotypes were identified for 26 of the 50 breeds, and haplotype sharing between some breeds indicated a common history R-M405 Haplotype Group. 132 likes · 2 talking about this. This a page to help discover and answer our R-M405 Haplotype Grou

Zhang, J, Vingron, M & Hoehe, MR 2001, On haplotype reconstruction for diploid populations.Report Eurandom, vol. 2001026, Eurandom, Eindhoven Aquaporin 4 (AQP4) in astrocytes facilitates a flow of cerebrospinal fluid between perivascular spaces and the brain parenchyma. This study shows that a common genetic haplotype linked to lower levels of AQP4 is associated with more intense NREM sleep and an improved response to extended wakefulness De novo approaches to haplotype-aware genome assembly Het genoom van een organisme omvat de complete genetische samenstelling en functioneert als een blauwdruk. Een genoom bestaat vaak uit meerdere kopieën, waarbij iedere kopie van één van de directe voorouders komt Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene Nellen, R. G. L., Steijlen, P. M., Hennies.

The Role of Beringia in the Global Dispersal of ModernMajor Histocompatibility Complex - WikiLectures
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