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Kidney International|September 18, 1997
Association of the angiotensin I converting enzyme gene deletion polymorphism with early onset of ESRF in PKD1 adult polycystic kidney diseaseK Baboolal, D Ravine, J Daniels, et al.Lancet (London, England)|April 2, 1994
Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1D Ravine, R N Gibson, R G Walker, et al.Lancet (London, England)|January 19, 1991
Treatable complications in undiagnosed cases of autosomal dominant polycystic kidney diseaseD Ravine, R G Walker, R N Gibson, et al.Journal of Medical Genetics|June 1, 1997
Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHDM Upadhyaya, J Maynard, M T Rogers, et al.Journal of Intellectual Disability Research : JIDR|December 4, 2003
Nurse recognition of early deviation in development in home videos of infants with Rett disorderB Burford, A M Kerr, H A MacleodBrain & Development|January 1, 1987
The hands, and the mind, pre- and post-regression, in Rett syndromeA M Kerr, J Montague, J B StephensonAmerican Journal of Medical Genetics|April 15, 1994
Nevoid basal cell carcinoma syndrome: review of 118 affected individualsS Shanley, J Ratcliffe, A Hockey, et al.Kidney International|September 29, 2001
Confirmation of a gene locus for medullary cystic kidney disease (MCKD2) on chromosome 16p12N Hateboer, C Gumbs, M D Teare, et al.Gut|September 22, 2005
Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patientsC A McCune, D Ravine, K Carter, et al.Developmental Medicine and Child Neurology|June 1, 1995
Visual function in Rett syndromeK J Saunders, D L McCulloch, A M KerrPageof 8