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Nature|January 3, 1991
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosomeC J Brown, A Ballabio, J L Rupert, et al.Experimental Cell Research|December 1, 1993
Correction of steroid sulfatase deficiency by gene transfer into basal cells of tissue-cultured epidermis from patients with recessive X-linked ichthyosisT G Jensen, U B Jensen, P K Jensen, et al.Optics Express|November 3, 2017
Analysis of Ge micro-cavities with in-plane tensile strains above 2R W Millar, K Gallacher, J Frigerio, et al.Genomics|February 28, 1998
Human FIGF: cloning, gene structure, and mapping to chromosome Xp22.1 between the PIGA and the GRPR genesM Rocchigiani, M Lestingi, A Luddi, et al.American Journal of Medical Genetics|September 6, 1996
Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: implication for the MRX locusK Muroya, T Ogata, N Matsuo, et al.Human Molecular Genetics|October 1, 1994
Expression of the Kallmann syndrome gene in human fetal brain and in the manipulated chick embryoB Lutz, S Kuratani, E I Rugarli, et al.Genomics|August 1, 1989
Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: implications for Norrie diseaseE R Levy, J F Powell, V J Buckle, et al.Molecular Psychiatry|September 29, 2004
Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphismsL M Butcher, E Meaburn, P S Dale, et al.Genomics|February 10, 1995
A bidirectional YAC walk from the Norrie disease (NDP) locusG C Black, M P Coleman, Z Y Chen, et al.Nature Genetics|October 1, 1993
A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathyZ Y Chen, E M Battinelli, A Fielder, et al.Pageof 30