Hoedjes et al 2014_Heredity_MemoryIntrogression

Dryad2014-01-01 更新2026-04-13 收录

行为遗传学

基因型-表型关联

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http://datadryad.org/resource/doi:10.5061/dryad.18v85/1 数据链接链接失效反馈

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Data from all memory retention test as described in the manuscript and results from the genotyping microarray.

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2014-01-01

Handedness and hand preference

利手研究

行为遗传学

The Netherlands Twin Register (NTR) consists of individuals who have agreed to participate in twin-family studies and was established and is managed by the Department of Biological Psychology, VU Univ

DataCite Commons2024-10-21 更新70

Family history of our cohort.

结肠直肠癌

基因型-表型关联

Pathogenic FLCN variant and clinical phenotype for each individual included in the study. FH: Family history, CRC: Colorectal cancer. (XLSX)

Figshare2022-02-17 更新10

Vc1218 Ins-18(Ok1672)I | 2011-05-17T10:49:00+01:00

秀丽隐杆线虫表型分析

行为遗传学

This experiment is part of the C.elegans behavioural database . For more information and the complete collection of experiments visit http://movement.openworm.org preview link : http

Zenodo2020-09-19 更新00

Fraction of simulated local heritability explained in WTCCC2 genotypes.

疾病遗传关联分析

基因型-表型关联

Analysis of simulated disease architecture with 180 causal 1Mbp loci yielding a true . In each locus, 1–10 causal variants were sampled from either low-frequency () of common (MAF) WTCCC2 SNPs. For ea

NIAID Data Ecosystem30

Supplementary Material for: Gray Matter Heterotopia, Mental Retardation, Developmental Delay, Microcephaly, and Facial Dysmorphisms in a Boy with Ring Chromosome 6: A 10-Year Follow-Up and Literature Review

环状染色体6

基因型-表型关联

Ring chromosome 6, r(6), is an extremely rare cytogenetic abnormality with clinical heterogeneity which arises typically de novo. The phenotypes of r(6) can be highly variable, ranging from almost nor

NIAID Data Ecosystem10

Hoedjes et al 2014_Heredity_MemoryIntrogression

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