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American Journal of Human Genetics|June 1, 1996
Parametric and nonparametric linkage analysis: a unified multipoint approachL Kruglyak, M J Daly, M P Reeve-Daly, et al.Human Genetics|October 13, 2000
Molecular genetic advances in tuberous sclerosisJ P Cheadle, M P Reeve, J R Sampson, et al.Epidemiology and Infection|March 31, 1999
Proteinuria is associated with persistence of antibody to streptococcal M protein in Aboriginal AustraliansA M Goodfellow, W E Hoy, K S Sriprakash, et al.Annals of Human Genetics|March 29, 2000
Superiority of denaturing high performance liquid chromatography over single-stranded conformation and conformation-sensitive gel electrophoresis for mutation detection in TSC2Y S Choy, S L Dabora, F Hall, et al.Cell|September 23, 1994
The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mappingJ Hästbacka, A de la Chapelle, M M Mahtani, et al.Genomics|December 1, 1994
Isolation and regional mapping of 110 chromosome 22 STSsT J Hudson, A M Colbert, M P Reeve, et al.Nature Genetics|November 1, 1996
The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and prunedR Saxena, L G Brown, T Hawkins, et al.Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Distinct and shared genetic architectures of Gestational diabetes mellitus and Type 2 Diabetes MellitusA Elliott, R K Walters, M Pirinen, et al.Nature|October 24, 1997
Serrate2 is disrupted in the mouse limb-development mutant syndactylismA Sidow, M S Bulotsky, A W Kerrebrock, et al.American Journal of Human Genetics|December 12, 2000
Mutational analysis in a cohort of 224 tuberous sclerosis patients indicates increased severity of TSC2, compared with TSC1, disease in multiple organsS L Dabora, S Jozwiak, D N Franz, et al.Pageof 2