Home › Biblio

Biblio

Found 3 results

2006
Hubbard WC, Moser AB, Tortorelli S, Liu A, Jones D, Moser H.  2006.  Combined liquid chromatography-tandem mass spectrometry as an analytical method for high throughput screening for X-linked adrenoleukodystrophy and other peroxisomal disorders: preliminary findings.. Molecular genetics and metabolism. 89(1-2):185-7. Abstract
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

Your Support is the Key

Submitted by admin on May 9, 2011 - 11:20am

Matthew Slattery

Help children like Matthew unlock their potential by becoming a Partner in Potential.

Donate Learn More