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American Journal of Human Genetics|February 1, 1995
Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37L C Wilson, K Leverton, M E Oude Luttikhuis, et al.American Journal of Human Genetics|February 1, 1995
A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12S Bleyl, L Nelson, S J Odelberg, et al.American Journal of Human Genetics|February 1, 1995
Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, D M Hallman, et al.American Journal of Human Genetics|February 1, 1995
Autosomal dominant distal myopathy: linkage to chromosome 14N G Laing, B A Laing, C Meredith, et al.American Journal of Human Genetics|February 1, 1995
Methods for genetic linkage analysis using trisomiesE Feingold, N E Lamb, S L ShermanAmerican Journal of Human Genetics|February 1, 1995
Breakpoint analysis: precise localization of genetic markers by means of nonstatistical computation using relatively few genotypesT I Elsner, H Albertsen, S C Gerken, et al.American Journal of Human Genetics|February 1, 1995
Two statistical tests for meiotic breakpoint analysisR Plaetke, G A SchachtelAmerican Journal of Human Genetics|March 1, 1995
An intragenic deletion of the P gene is the common mutation causing tyrosinase-positive oculocutaneous albinism in southern African NegroidsG Stevens, J van Beukering, T Jenkins, et al.American Journal of Human Genetics|March 1, 1995
Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypesH M Mitchison, A M O'Rawe, P E Taschner, et al.American Journal of Human Genetics|March 1, 1995
Delivery of molecular genetic services within a health care system: time analysis of the clinical workload. The Molecular Genetic Study GroupL C Surh, P G Wright, M Cappelli, et al.Pageof 980