Showing results (4411-4420 of 7,440) with videos related to
Sort By:
Pageof 744
Nature Genetics|October 1, 1995
Frequency of homozygous deletion at p16/CDKN2 in primary human tumoursP Cairns, T J Polascik, Y Eby, et al.Nature Genetics|October 1, 1995
Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophyA Helbling-Leclerc, X Zhang, H Topaloglu, et al.Nature Genetics|May 1, 1995
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductaseP Frosst, H J Blom, R Milos, et al.Nature Genetics|May 1, 1995
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2H A Phillips, I E Scheffer, S F Berkovic, et al.Nature Genetics|May 1, 1995
A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosisP W Reymer, E Gagné, B E Groenemeyer, et al.Nature Genetics|May 1, 1995
Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutaseP M Andersen, P Nilsson, V Ala-Hurula, et al.Nature Genetics|May 1, 1995
The reeler gene encodes a protein with an EGF-like motif expressed by pioneer neuronsS Hirotsune, T Takahara, N Sasaki, et al.Nature Genetics|May 1, 1995
Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individualsA Servadio, B Koshy, D Armstrong, et al.Nature Genetics|June 1, 1995
Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activityJ K Naggert, L D Fricker, O Varlamov, et al.Pageof 744