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International Journal of Obesity (2005)|April 10, 2013
Roux-en-Y gastric bypass normalizes the blunted postprandial bile acid excursion associated with obesityN N Ahmad, A Pfalzer, L M KaplanJournal of Medical Genetics|February 1, 1995
Modification of standard proteinase K/phenol method for DNA isolation to improve yield and purity from frozen bloodN N Ahmad, A B Cu-Unjieng, L A DonosoArchives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1995
Stickler syndrome. A mutation in the nonhelical 3' end of type II procollagen geneN N Ahmad, J Dimascio, R G Knowlton, et al.Ophthalmic Genetics|January 5, 2000
A possible hot spot in exon 21 of the retinoblastoma gene predisposing to a low penetrant retinoblastoma phenotype?N N Ahmad, M B Melo, A D Singh, et al.Journal of Medical Genetics|August 1, 1996
PCR assay confirms diagnosis in syndrome with variably expressed phenotype: mutation detection in Stickler syndromeN N Ahmad, D M McDonald-McGinn, P Dixon, et al.Leukemia Research|August 26, 1998
Molecular analysis of the retinoblastoma (RB1) gene in acute myeloid leukemia patientsM B Melo, F F Costa, S T Saad, et al.American Journal of Human Genetics|January 1, 1993
A second mutation in the type II procollagen gene (COL2AI) causing stickler syndrome (arthro-ophthalmopathy) is also a premature termination codonN N Ahmad, D M McDonald-McGinn, E H Zackai, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy)N N Ahmad, L Ala-Kokko, R G Knowlton, et al.Human Mutation|January 1, 1992
Detection of sequence variants in the gene for human type II procollagen (COL2A1) by direct sequencing of polymerase chain reaction-amplified genomic DNAC J Williams, D A Harrison, I Hopkinson, et al.Pageof 1