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Human Molecular Genetics|September 25, 1997
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the regionM D'Esposito, M R Matarazzo, A Ciccodicola, et al.Clinical Genetics|November 27, 1998
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneityG de Crecchio, F Simonelli, G Nunziata, et al.Journal of Human Genetics|June 4, 1998
The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32M Fujimoto, P N Kantaputra, S Ikegawa, et al.Human Mutation|July 20, 2001
Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domainsM G Miano, F Testa, F Filippini, et al.Genomics|December 1, 1991
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28D Schlessinger, R D Little, D Freije, et al.Nature Genetics|May 1, 1996
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)A Meindl, K Dry, K Herrmann, et al.European Journal of Human Genetics : EJHG|September 14, 1999
Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosaM G Miano, F Testa, M Strazzullo, et al.Human Molecular Genetics|February 3, 2000
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal regionA Ciccodicola, M D'Esposito, T Esposito, et al.Journal of Molecular Medicine (Berlin, Germany)|March 28, 2001
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome femalesM Vacca, F Filippini, A Budillon, et al.Brain & Development|December 12, 2001
MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved regionM Vacca, F Filippini, A Budillon, et al.Pageof 10