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Nature Genetics|February 1, 1995
Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor geneH Kremer, R Kraaij, S P Toledo, et al.Human Molecular Genetics|October 1, 1992
Mutations in the candidate gene for Norrie diseaseW Berger, D van de Pol, M Warburg, et al.Human Genetics|November 1, 1996
Localization of the gene (or genes) for a syndrome with X-linked mental retardation, ataxia, weakness, hearing impairment, loss of vision and a fatal course in early childhoodH Kremer, B C Hamel, B van den Helm, et al.Human Molecular Genetics|June 1, 1996
Identification of a gene disrupted by a microdeletion in a patient with X-linked retinitis pigmentosa (XLRP)R Roepman, D Bauer, T Rosenberg, et al.Human Molecular Genetics|November 1, 1993
Cosegregation of missense mutations of the luteinizing hormone receptor gene with familial male-limited precocious pubertyH Kremer, E Mariman, B J Otten, et al.Genomics|June 1, 1992
Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panelH Traupe, A M van den Ouweland, B A van Oost, et al.Genes, Chromosomes & Cancer|March 1, 1993
Identification of a yeast artificial chromosome (YAC) spanning the synovial sarcoma-specific t(X;18)(p11.2;q11.2) breakpointB de Leeuw, W Berger, R J Sinke, et al.Nature Genetics|June 1, 1992
Isolation of a candidate gene for Norrie disease by positional cloningW Berger, A Meindl, T J van de Pol, et al.American Journal of Human Genetics|October 1, 1988
Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal XqF P Cremers, T J van de Pol, B Wieringa, et al.Human Molecular Genetics|May 1, 1992
An autosomal homologue of the choroideremia gene colocalizes with the Usher syndrome type II locus on the distal part of chromosome 1qF P Cremers, C M Molloy, D J van de Pol, et al.Pageof 21