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Kidney International|July 20, 1999
Familial phenotype differences in PKD11N Hateboer, L P Lazarou, A J Williams, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 31, 2000
Co-occurrence of autosomal dominant polycystic kidney disease and Marfan syndrome in a kindredN Hateboer, M Buchalter, S J Davies, et al.Human Genetics|April 1, 1998
Novel and recurrent mutations in the PKD1 (polycystic kidney disease) geneC Daniells, M Maheshwar, L Lazarou, et al.American Journal of Medical Genetics|October 23, 1997
Dominant coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palateD Ravine, N K Ragge, D Stephens, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|April 30, 2003
Sporadic case of fatal encephalopathy with neonatal onset associated with a T158M missense mutation in MECP2S A Lynch, S D Whatley, V Ramesh, et al.Archives of Disease in Childhood|March 23, 1999
Growth in Sotos syndromeJ C Agwu, N J Shaw, J Kirk, et al.British Medical Journal (Clinical Research Ed.)|August 31, 1985
Rett's syndrome in the west of ScotlandA M Kerr, J B StephensonAmerican Journal of Medical Genetics. Supplement|January 1, 1986
A study of the natural history of Rett syndrome in 23 girlsA M Kerr, J B StephensonArchives of Disease in Childhood|May 27, 2010
Valproate and risk of fracture in Rett syndromeH Leonard, J Downs, L Jian, et al.Pageof 8