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Ophthalmic Paediatrics and Genetics|August 1, 1986
Retinal neovascularization in Potter's syndrome secondary to renal agenesisD H Adkins, A H Bunt-Milam, R A PagonOphthalmic Paediatrics and Genetics|August 1, 1986
'Leopard spot' retinopathy in Warburg syndromeR A Barth, R A Pagon, A H Bunt-MilamThe Journal of Pediatrics|April 6, 1999
Phenotypic spectrum and management issues in Kabuki syndromeH Kawame, M C Hannibal, L Hudgins, et al.Investigative Ophthalmology & Visual Science|April 1, 1983
Clinical-ultrastructural study of a retinal dystrophyA H Bunt-Milam, R E Kalina, R A PagonHuman Genetics|January 1, 1984
X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypesC M Disteche, K Swisshelm, S Forbes, et al.Journal of Medical Genetics|August 1, 1985
Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorderR A Pagon, T D Bird, J C Detter, et al.Gastroenterology|April 1, 1988
Visceral myopathy of the gastrointestinal and genitourinary tracts in infantsM D Schuffler, R A Pagon, R Schwartz, et al.Developmental Medicine and Child Neurology|April 1, 1996
Marinesco-Sjögren syndrome: clinical and magnetic resonance imaging features in three childrenJ F McLaughlin, R A Pagon, E Weinberger, et al.American Journal of Medical Genetics|March 3, 1997
Facio-oculo-acoustico-renal (FOAR) syndrome: case report and reviewD B Schowalter, R A Pagon, R E Kalina, et al.Developmental Medicine and Child Neurology|July 1, 1996
Marinesco-Sjögren syndrome: clinical and magnetic resonance imaging features in three childrenJ F McLaughlin, R A Pagon, E Weinberger, et al.Pageof 37