Showing results (501-510 of 7,414) with videos related to
Sort By:
Pageof 742
Nature Genetics|July 1, 1993
The gene for Machado-Joseph disease maps to human chromosome 14qY Takiyama, M Nishizawa, H Tanaka, et al.Nature Genetics|July 1, 1993
Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11L Carrier, C Hengstenberg, J S Beckmann, et al.Nature Genetics|July 1, 1993
Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patientsF Taroni, E Verderio, F Dworzak, et al.Nature Genetics|January 1, 1993
Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigreesM Baron, N F Freimer, N Risch, et al.Nature Genetics|January 1, 1993
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPaseC Vulpe, B Levinson, S Whitney, et al.Nature Genetics|January 1, 1993
Independent mutations of the human CD3-epsilon gene resulting in a T cell receptor/CD3 complex immunodeficiencyC Soudais, J P de Villartay, F Le Deist, et al.Nature Genetics|January 1, 1993
Structure and physical map of 64 variable segments in the 3'0.8-megabase region of the human immunoglobulin heavy-chain locusF Matsuda, E K Shin, H Nagaoka, et al.Nature Genetics|February 1, 1993
Towards gene therapy for haemophilia B using primary human keratinocytesA J Gerrard, D L Hudson, G G Brownlee, et al.Nature Genetics|March 1, 1993
Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS geneB E Nichols, V C Sheffield, K Vandenburgh, et al.Nature Genetics|March 1, 1993
A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescensK Kajiwara, M A Sandberg, E L Berson, et al.Pageof 742