Showing results (1631-1640 of 9,569) with videos related to
Sort By:
Pageof 957
Human Genetics|April 6, 2002
The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup JMichael D Brown, Elena Starikovskaya, Olga Derbeneva, et al.Human Genetics|April 6, 2002
Evidence of multiple causal sites affecting weight in the IGF2-INS-TH region of human chromosome 11Dongfeng Gu, Sandra D O'Dell, Xiao-he Chen, et al.Human Genetics|April 6, 2002
Variability of X chromosome inactivation: effect on levels of TIMP1 RNA and role of DNA methylationCatherine L Anderson, Carolyn J BrownHuman Genetics|December 22, 2009
Examination of FGFRL1 as a candidate gene for diaphragmatic defects at chromosome 4p16.3 shows that Fgfrl1 null mice have reduced expression of Tpm3, sarcomere genes and Lrtm1 in the diaphragmNelson LopezJimenez, Simon Gerber, Vlad Popovici, et al.Human Genetics|January 8, 2010
Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23–22.3Gul Naz, Ghazanfar Ali, Syed Kamran-ul-Hassan Naqvi, et al.Human Genetics|December 26, 2009
Genetic and functional analysis of common MRC1 exon 7 polymorphisms in leprosy susceptibilityAndrea Alter, Louis de Léséleuc, Nguyen Van Thuc, et al.Human Genetics|January 20, 2010
Significant association of glutamate receptor, ionotropic N-methyl-D-aspartate 3A (GRIN3A), with nicotine dependence in European- and African-American smokersJennie Z Ma, Thomas J Payne, Justin Nussbaum, et al.Human Genetics|April 1, 1994
Amplification of (GACA)n simple repeats in an exceptional 14p+ marker chromosomeM Schmid, I Nanda, C Steinlein, et al.Human Genetics|April 1, 1994
Incidence of chromosome 18 disomy in human sperm nuclei as detected by nonisotopic in situ hybridizationM Guttenbach, R Schakowski, M SchmidHuman Genetics|April 1, 1994
Mutational analysis of the amyloid precursor protein gene in Japanese familial Alzheimer's disease kindredsH Fujigasaki, S Naruse, K Kaneko, et al.Pageof 957