Showing results (2201-2210 of 7,438) with videos related to
Sort By:
Pageof 744
Nature Genetics|July 1, 1995
Establishment of functional imprinting of the H19 gene in human developing placentaeY Jinno, Y Ikeda, K Yun, et al.Nature Genetics|July 1, 1995
Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasiaJ T Hecht, L D Nelson, E Crowder, et al.Nature Genetics|July 1, 1995
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasiaG A Bellus, I McIntosh, E A Smith, et al.Nature Genetics|August 1, 1995
The renal glomerulus of mice lacking s-laminin/laminin beta 2: nephrosis despite molecular compensation by laminin beta 1P G Noakes, J H Miner, M Gautam, et al.Nature Genetics|August 1, 1995
Distinct genetic loci control development of benign and malignant skin tumours in miceH Nagase, S Bryson, H Cordell, et al.Nature Genetics|August 1, 1995
Gene therapy of metastatic cancer by in vivo retroviral gene targetingR K Hurford, G Dranoff, R C Mulligan, et al.Nature Genetics|August 1, 1995
Different chromosomal localization of the Clcn4 gene in Mus spretus and C57BL/6J miceE I Rugarli, D A Adler, G Borsani, et al.Nature Genetics|August 1, 1995
Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndromeK A Lugenbeel, A M Peier, N L Carson, et al.Nature Genetics|June 1, 1995
A subset of p53-deficient embryos exhibit exencephalyV P Sah, L D Attardi, G J Mulligan, et al.Nature Genetics|June 1, 1995
p53 modulation of TFIIH-associated nucleotide excision repair activityX W Wang, H Yeh, L Schaeffer, et al.Pageof 744