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Annals of Human Genetics|September 4, 2018
Update of spectrum c.35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing lossFatemeh Azadegan-Dehkordi, Reza Ahmadi, Mahbobeh Koohiyan, et al.
Annals of Human Genetics|July 30, 2019
SIRT1 gene polymorphisms are associated with nondiabetic type 1 cardiorenal syndromeJiebin Hou, Xinyue Xie, Qingxian Tu, et al.
Annals of Human Genetics|February 12, 2021
Crosstalk between miR-203 and PKCθ regulates breast cancer stem cell markersSohair Salem, Rehab Mosaad
Annals of Human Genetics|February 17, 2017
Strong Amerindian Mitonuclear Discordance in Puerto Rican Genomes Suggests Amerindian Mitochondrial BenefitSteven E Massey
Annals of Human Genetics|October 5, 2019
In silico analysis of nonsynonymous single-nucleotide polymorphisms (nsSNPs) of the SMPX geneMd Arifuzzaman, Sarmistha Mitra, Raju Das, et al.
Annals of Human Genetics|September 10, 2019
A homozygous mutation in CMAS causes autosomal recessive intellectual disability in a Kazakh familyRonggui Qu, Qing Sang, Xueqian Wang, et al.
Annals of Human Genetics|July 11, 1998
Population paths implied by the mean number of pairwise nucleotide differences among mitochondrial DNA sequencesN Bonneuil
Annals of Human Genetics|December 16, 2004
The FBN1 (R2726W) mutation is not fully penetrantS Buoni, R Zannolli, F Macucci, et al.
Annals of Human Genetics|January 11, 2005
Double heterozygosity with mutations involving both the GJB2 and GJB6 genes is a possible, but very rare, cause of congenital deafness in the Czech populationP Seeman, O Bendová, D Rasková, et al.
Annals of Human Genetics|January 11, 2005
Linkage analysis of chromosome 1 with essential hypertension and blood pressure quantitative traits in Chinese familiesD Ge, J Huang, W Yang, et al.
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