Showing results (1711-1720 of 9,792) with videos related to
Sort By:
Pageof 980
American Journal of Human Genetics|November 1, 1986
Chromatid repulsion associated with Roberts/SC phocomelia syndrome is reduced in malignant cells and not expressed in interspecies somatic-cell hybridsN E Krassikoff, J M Cowan, D M Parry, et al.American Journal of Human Genetics|November 1, 1986
Paternal age and the occurrence of birth defectsZ H Lian, M M Zack, J D EricksonAmerican Journal of Human Genetics|November 1, 1986
High molecular weight DNA from fixed cytogenetic preparationsP E Barker, J R Testa, N Z Parsa, et al.American Journal of Human Genetics|March 1, 1985
Role of the apolipoprotein E polymorphism in determining normal plasma lipid and lipoprotein variationC F Sing, J DavignonAmerican Journal of Human Genetics|March 1, 1985
Paternal-age and birth-order effect on the human secondary sex ratioA RuderAmerican Journal of Human Genetics|August 25, 2022
Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrationsVikrant Kumar, Richard B Pouw, Matias I Autio, et al.American Journal of Human Genetics|June 11, 2025
Bi-allelic mutations in FASTKD5 are associated with cytochrome c oxidase deficiency and early- to late-onset Leigh syndromeHana Antonicka, Woranontee Weraarpachai, Katherine M Szigety, et al.American Journal of Human Genetics|May 31, 2025
Bi-allelic variants in TM2D3 cause a severe syndromic neurodevelopmental disorder associated with endoplasmic reticulum and mitochondrial abnormalitiesClaudie Gabillard-Lefort, Caroline Silveira Martinez, Naïg Gueguen, et al.American Journal of Human Genetics|June 6, 2025
Consultation informs strategies for improving the use of functional evidence in variant classificationRehan M Villani, Bronwyn Terrill, Emma Tudini, et al.American Journal of Human Genetics|October 7, 2025
A scalable approach for genomic-first rare disorder detection in a healthcare-based populationRebecca I Torene, Karyn Meltz Murphy, Tracy Brandt, et al.Pageof 980