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Pediatric Nephrology (Berlin, Germany)|July 1, 1988
The application of molecular biology to the prenatal diagnosis of renal diseaseF A Flinter, M BobrowGenomics|April 1, 1989
Localization of the gene for classic Alport syndromeF A Flinter, S Abbs, M BobrowAmerican Journal of Medical Genetics. Part A|June 5, 2003
Terminal deletion of chromosome 5p in a patient with phenotypical features of Lujan-Fryns syndromeE Stathopulu, C Mackie Ogilvie, F A FlinterHuman Mutation|March 27, 1999
Detection of mutations in COL4A5 in patients with Alport syndromeK E Plant, P M Green, D Vetrie, et al.Journal of Medical Genetics|May 1, 1993
Probable de novo 17q duplication (q11.2-->q21.1): a newly recognised chromosomal syndrome in a child with Klinefelter's syndromeA M Butt, D Mehta, J A Goodeve, et al.Clinical Dysmorphology|January 1, 1997
Phenotypic diversity in the Smith-Lemli-Opitz syndromeM J Seller, F A Flinter, Z Docherty, et al.Lancet (London, England)|October 29, 1988
Genetics of classic Alport's syndromeF A Flinter, J S Cameron, C Chantler, et al.Human Reproduction (Oxford, England)|October 27, 2001
Robertsonian translocations--reproductive risks and indications for preimplantation genetic diagnosisP N Scriven, F A Flinter, P R Braude, et al.Journal of Medical Genetics|June 30, 2000
New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population surveyP L Beales, N Elcioglu, A S Woolf, et al.Human Reproduction (Oxford, England)|March 29, 2011
Meiotic segregation of Robertsonian translocations ascertained in cleavage-stage embryos--implications for preimplantation genetic diagnosisS M Bint, C Mackie Ogilvie, F A Flinter, et al.Pageof 2