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Biblio

Found 4 results

2010
Zhang R, Chen L, Jiralerspong S, Snowden A, Steinberg S, Braverman N.  2010.  Recovery of PEX1-Gly843Asp peroxisome dysfunction by small-molecule compounds.. Proceedings of the National Academy of Sciences of the United States of America. 107(12):5569-74. Abstract
2008
Mardo V, Squibb EE, Braverman N, Hoover-Fong JE, Migeon C, Batista DAS, Thomas GH.  2008.  Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for genital development.. American journal of medical genetics. Part A. 146A(17):2293-7.
2005
Naidu S, Bibat G, Lin D, Burger P, Barker P, Rosemberg S, Braverman N, Arroyo H, Dowling M, Hamosh A et al..  2005.  Progressive cavitating leukoencephalopathy: a novel childhood disease.. Annals of neurology. 58(6):929-38. Abstract
2004
Steinberg S, Chen L, Wei L, Moser A, Moser H, Cutting G, Braverman N.  2004.  The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.. Molecular genetics and metabolism. 83(3):252-63. Abstract

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