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Journal of Human Genetics|September 18, 2001
The T911C (F304S) substitution in the human ALG6 gene is a common polymorphism and not a causal mutation of CDG-IcS Vuillaumier-Barrot, C Le Bizec, G Durand, et al.Journal of Human Genetics|September 18, 2001
Single nucleotide polymorphisms of the resistin (RSTN) geneH Cao, R A HegeleJournal of Human Genetics|July 12, 2002
Homozygous deletion on the chromosomal region 5q12.3 in human lines of small-cell lung cancersKenji Tamura, Wataru Miwa, Tomoko Maruyama, et al.Journal of Human Genetics|July 12, 2002
Strategies for genome-wide association studies: optimization of study designs by the stepwise focusing methodAkira Saito, Naoyuki KamataniJournal of Human Genetics|July 12, 2002
Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseasesMasaji Tachikawa, Yoshitaka Nagai, Koichiro Nakamura, et al.Journal of Human Genetics|July 12, 2002
Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 ( ABCA1) gene in Japanese patients with Tangier diseaseZhigang Guo, Akihiro Inazu, Wenxin Yu, et al.Journal of Human Genetics|May 29, 2002
Microdeletions of a Y-specific marker, Yfm1, and implications for a role in spermatogenesisAshraf A Ewis, Juwon Lee, Toshikatsu Shinka, et al.Journal of Human Genetics|July 29, 2021
Genetics of autosomal mosaic chromosomal alteration (mCA)Xiaoxi Liu, Yoichiro Kamatani, Chikashi TeraoJournal of Human Genetics|October 28, 2016
Molecular analysis of 23 Pakistani families with autosomal recessive primary microcephaly using targeted next-generation sequencingRongrong Wang, Amjad Khan, Shirui Han, et al.Journal of Human Genetics|November 25, 2016
A combined linkage and association strategy identifies a variant near the GSTP1 gene associated with BMI in the Mexican populationHugo Villamil-Ramírez, Paola León-Mimila, Luis R Macias-Kauffer, et al.Pageof 353