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Human Genetics|December 24, 1997
Novel stop and frameshifting mutations in the autosomal dominant polycystic kidney disease 2 (PKD2) geneM Viribay, T Hayashi, D Tellería, et al.European Journal of Human Genetics : EJHG|February 15, 2001
Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TELJ Brown, S W Horsley, C Jung, et al.American Journal of Human Genetics|June 1, 1990
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3A O Wilkie, V J Buckle, P C Harris, et al.Genomics|September 15, 1994
A large duplicated area in the polycystic kidney disease 1 (PKD1) region of chromosome 16 is prone to rearrangementP C Harris, S Thomas, A B MacCarthy, et al.American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 21, 2010
Therapeutic mTOR inhibition in autosomal dominant polycystic kidney disease: What is the appropriate serum level?G Canaud, B Knebelmann, P C Harris, et al.Human Molecular Genetics|November 7, 2000
A human PKD1 transgene generates functional polycystin-1 in mice and is associated with a cystic phenotypeL Pritchard, J A Sloane-Stanley, J A Sharpe, et al.Genomics|September 24, 1999
Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16qB J Loftus, U J Kim, V P Sneddon, et al.Pageof 16