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Human Molecular Genetics|July 1, 1997
The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3S A Feather, A S Woolf, D Donnai, et al.Lancet (London, England)|April 2, 1988
Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiencyJ Goodship, S Malcolm, Y L Lau, et al.Blood|June 15, 1991
Carrier detection in Wiskott-Aldrich syndrome: combined use of M27 beta for X-inactivation studies and as a linked probeJ Goodship, J Carter, T Espanol, et al.American Journal of Human Genetics|January 1, 1990
Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17H R Middleton-Price, A E Harding, C Monteiro, et al.Free Radical Biology & Medicine|February 3, 2000
Characterization of iodoacetate-mediated neurotoxicity in vitro using primary cultures of rat cerebellar granule cellsC S Malcolm, K R Benwell, H Lamb, et al.Journal of Medical Genetics|December 14, 1999
Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32M M Lees, R M Winter, S Malcolm, et al.Canadian Journal of Microbiology|July 1, 1983
Colony counting on hydrophobic grid-membrane filtersA N Sharpe, M P Diotte, I Dudas, et al.Artificial Cells, Blood Substitutes, and Immobilization Biotechnology|January 1, 1994
Characterization of the hemodynamic response to intravenous diaspirin crosslinked hemoglobin solution in ratsD S Malcolm, I N Hamilton, S C Schultz, et al.American Journal of Human Genetics|January 1, 1991
Chromosome 15 uniparental disomy is not frequent in Angelman syndromeJ H Knoll, K A Glatt, R D Nicholls, et al.Tissue Antigens|March 1, 1981
New HLA-D alleles associated with DR1 and DR2N Suciu-Foca, M Godfrey, G Khan, et al.Pageof 32