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H Lipson

Showing results (81-90 of 99) with videos related to

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Journal of Medical Genetics|September 1, 1991
Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recogniseA H Lipson, D Yuille, M Angel, et al.
Prenatal Diagnosis|May 18, 1999
Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiencyK M Brookhyser, M H Lipson, A B Moser, et al.
American Journal of Medical Genetics|December 25, 1991
Radiological findings in Hallermann-Streiff syndrome: report of five cases and a review of the literatureC L Christian, R S Lachman, A S Aylsworth, et al.
Australian and New Zealand Journal of Ophthalmology|August 1, 1990
The eye and the hand: a clinical reviewT V Roberts, I C Francis, A H Lipson, et al.
The American Journal of Clinical Nutrition|February 1, 1994
Decreased bone mineral density in children with phenylketonuriaJ R Allen, I R Humphries, D L Waters, et al.
American Journal of Medical Genetics|September 11, 1995
Prenatal exposure to phenytoin, facial development, and a possible role for vitamin KA M Howe, A H Lipson, L J Sheffield, et al.
Human Mutation|January 1, 1997
Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)R A Spritz, S T Lee, K Fukai, et al.
Journal of Human Genetics|October 21, 2011
Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysisGanka V Douglas, Joanna Wiszniewska, Mark H Lipson, et al.
Molecular Genetics and Metabolism|March 24, 2010
Maple syrup urine disease: further evidence that newborn screening may fail to identify variant formsR L Puckett, F Lorey, P Rinaldo, et al.
Pediatric Dermatology|February 1, 1988
Ruvalcaba-Myhre-Smith syndromeJ C Gretzula, O Hevia, L S Schachner, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|September 1, 1991
Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recogniseA H Lipson, D Yuille, M Angel, et al.
Prenatal Diagnosis|May 18, 1999
Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiencyK M Brookhyser, M H Lipson, A B Moser, et al.
American Journal of Medical Genetics|December 25, 1991
Radiological findings in Hallermann-Streiff syndrome: report of five cases and a review of the literatureC L Christian, R S Lachman, A S Aylsworth, et al.
Australian and New Zealand Journal of Ophthalmology|August 1, 1990
The eye and the hand: a clinical reviewT V Roberts, I C Francis, A H Lipson, et al.
The American Journal of Clinical Nutrition|February 1, 1994
Decreased bone mineral density in children with phenylketonuriaJ R Allen, I R Humphries, D L Waters, et al.
American Journal of Medical Genetics|September 11, 1995
Prenatal exposure to phenytoin, facial development, and a possible role for vitamin KA M Howe, A H Lipson, L J Sheffield, et al.
Human Mutation|January 1, 1997
Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)R A Spritz, S T Lee, K Fukai, et al.
Journal of Human Genetics|October 21, 2011
Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysisGanka V Douglas, Joanna Wiszniewska, Mark H Lipson, et al.
Molecular Genetics and Metabolism|March 24, 2010
Maple syrup urine disease: further evidence that newborn screening may fail to identify variant formsR L Puckett, F Lorey, P Rinaldo, et al.
Pediatric Dermatology|February 1, 1988
Ruvalcaba-Myhre-Smith syndromeJ C Gretzula, O Hevia, L S Schachner, et al.
Pageof 10