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Human Genetics|December 18, 2008
Identification of genomic regions contributing to etoposide-induced cytotoxicityWasim K Bleibel, Shiwei Duan, R Stephanie Huang, et al.Human Genetics|December 15, 1976
Hereditary hemolytic anemia with erythrocyte pyrimidine 5'-nucleotidase deficiency in Spain. Clinical, biological and familial studiesJ L Vives-Corrons, E Montserrat-Costa, C RozmanHuman Genetics|August 19, 2008
Somatic mosaicism for a PDHA1 mutation in a female with pyruvate dehydrogenase deficiencyCheryl K Ridout, Ruth M Brown, John H Walter, et al.Human Genetics|October 14, 2008
Missing data imputation and haplotype phase inference for genome-wide association studiesSharon R BrowningHuman Genetics|December 24, 2008
Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4)N Simon Thomas, Viv Maloney, Victoria Bryant, et al.Human Genetics|December 25, 2008
Population admixture associated with disease prevalence in the Boston Puerto Rican health studyChao-Qiang Lai, Katherine L Tucker, Shweta Choudhry, et al.Human Genetics|October 3, 2008
A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2-q26.33Xiao-Hua Dai, Wen-Wu Chen, Xu Wang, et al.Human Genetics|October 19, 2007
Evidence for linkage of a new region (11p14) to eczema and allergic diseasesMichel Guilloud-Bataille, Emmanuelle Bouzigon, Isabella Annesi-Maesano, et al.Human Genetics|October 10, 2007
Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14Hui Li, Jia-Xin Wang, Cheng-Ye Wang, et al.Human Genetics|September 29, 2007
Discovering DNA: Friedrich Miescher and the early years of nucleic acid researchRalf DahmPageof 958