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Annals of Human Genetics|March 26, 2014
Complete mitochondrial genome analysis and clinical documentation of a five-generational Indian family with mitochondrial 1555A>G mutation and postlingual hearing lossMahalingam Subathra, Mathiyalagan Selvakumari, Arabandi Ramesh, et al.Annals of Human Genetics|February 28, 2014
Utilising family-based designs for detecting rare variant disease associationsMark D Preston, Frank DudbridgeAnnals of Human Genetics|March 14, 2014
Maternal genetic heritage of Southeastern Europe reveals a new Croatian isolate and a novel, local sub-branching in the x2 haplogroupJelena Sarac, Tena Sarić, Dubravka Havaš Auguštin, et al.Annals of Human Genetics|March 14, 2014
Promoter methylation of the RASSF1A gene may contribute to colorectal cancer susceptibility: a meta-analysis of cohort studiesHe-Ling Wang, Peng Liu, Ping-Yi Zhou, et al.Annals of Human Genetics|July 1, 1986
Immunological cross-reactivity of alcohol dehydrogenase (ADH) isozymes with rabbit immune sera against horse and human ADH subunitsA Adinolfi, O Massa, G d'AlessandroAnnals of Human Genetics|May 23, 2008
Identifying modifier loci in existing genome scan dataE W Daw, Y Lu, A J Marian, et al.Annals of Human Genetics|August 31, 2019
A novel mutation of MSX1 inherited from maternal mosaicism causes a severely affected child with nonsyndromic oligodontiaTengfei Ma, Yi Liu, Xiaoxue Zhao, et al.Annals of Human Genetics|September 13, 2019
GJB2-related hearing loss in central Iran: Review of the spectrum and frequency of gene mutationsMahbobeh Koohiyan, Farideh Koohian, Fatemeh Azadegan-DehkordiAnnals of Human Genetics|August 3, 2019
Shared gene signature between pterygium and meibomian gland dysfunction uncovered through gene-expression meta-analysisJing Zhang, Jun Xiang, Dan Wu, et al.Pageof 231