Showing results (2751-2760 of 9,791) with videos related to
Sort By:
Pageof 980
American Journal of Human Genetics|November 1, 1996
Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the diseaseE Hahnen, J Schönling, S Rudnik-Schöneborn, et al.American Journal of Human Genetics|November 1, 1996
Genomic imprinting of the human serotonin-receptor (HTR2) gene involved in development of retinoblastomaM V Kato, T Shimizu, M Nagayoshi, et al.American Journal of Human Genetics|November 1, 1996
Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16G Tromp, H Kuivaniemi, S Raphael, et al.American Journal of Human Genetics|November 1, 1996
Sex ratio in normal and disomic sperm: evidence that the extra chromosome 21 preferentially segregates with the Y chromosomeD K Griffin, M A Abruzzo, E A Millie, et al.American Journal of Human Genetics|November 1, 1996
Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q)F Bernasconi, A Karagüzel, F Celep, et al.American Journal of Human Genetics|November 1, 1996
The role of HLA class II genes in insulin-dependent diabetes mellitus: molecular analysis of 180 Caucasian, multiplex familiesJ A Noble, A M Valdes, M Cook, et al.American Journal of Human Genetics|October 1, 1996
Genetic recombination at the human RH locus: a family study of the red-cell Evans phenotype reveals a transfer of exons 2-6 from the RHD to the RHCE geneC H Huang, Y Chen, M Reid, et al.American Journal of Human Genetics|October 1, 1996
Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5G van der Steege, P M Grootscholten, J M Cobben, et al.American Journal of Human Genetics|October 1, 1996
Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotypeM Al-Maghtheh, E Vithana, E Tarttelin, et al.American Journal of Human Genetics|October 1, 1996
Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotypeT Weiler, C R Greenberg, E Nylen, et al.Pageof 980