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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Disease and CHD1L[original query]
Human gene copy number spectra analysis in congenital heart malformations.
Physiological genomics 2012 Feb .
Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME
Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data.
PloS one 2013 8 (12): e81503.
Mosley Jonathan D, Van Driest Sara L, Larkin Emma K, Weeke Peter E, Witte John S, Wells Quinn S, Karnes Jason H, Guo Yan, Bastarache Lisa, Olson Lana M, McCarty Catherine A, Pacheco Jennifer A, Jarvik Gail P, Carrell David S, Larson Eric B, Crosslin David R, Kullo Iftikhar J, Tromp Gerard, Kuivaniemi Helena, Carey David J, Ritchie Marylyn D, Denny Josh C, Roden Dan
Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary Tract.
Journal of clinical medicine 2020 3 9 (3): .
Ahn Yo Han, Lee Chung, Kim Nayoung K D, Park Eujin, Kang Hee Gyung, Ha Il-Soo, Park Woong-Yang, Cheong Hae
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