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Human Molecular Genetics|January 1, 1996
An animal model for Norrie disease (ND): gene targeting of the mouse ND geneW Berger, D van de Pol, D Bächner, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Evidence against a major role of PEG1/MEST in Silver-Russell syndromeA M Riesewijk, N Blagitko, A A Schinzel, et al.Kidney International|October 1, 1988
Localization of the gene for X-linked Alport's syndromeH Brunner, C Schröder, C van Bennekom, et al.Human Genetics|September 1, 1987
An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 regionF P Cremers, R A Pfeiffer, T J van de Pol, et al.Human Molecular Genetics|November 1, 1995
A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 geneY J de Kok, G F Merkx, S M van der Maarel, et al.Human Molecular Genetics|July 1, 1994
Cloning and characterization of the human choroideremia geneH van Bokhoven, J A van den Hurk, L Bogerd, et al.Journal of Medical Genetics|December 1, 1994
Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal familiesM Bitner-Glindzicz, Y de Kok, D Summers, et al.Somatic Cell and Molecular Genetics|January 1, 1994
Radiation hybrids for the proximal long arm of the X chromosome and their use in the derivation of an ordered set of cosmid markers from a defined subregion in proximal Xq13.1D Röhme, T Sidén, S M van der Maarel, et al.Genomics|August 1, 1988
The poliovirus sensitivity (PVS) gene is on chromosome 19q12----q13.2T Siddique, R McKinney, W Y Hung, et al.Human Molecular Genetics|May 1, 1994
Molecular cloning of the synovial sarcoma-specific translocation (X;18)(p11.2;q11.2) breakpointB de Leeuw, M Balemans, D O Weghuis, et al.Pageof 21