NDLI: Peroxisomal disorders: clinical and biochemical studies in 15 children and prenatal diagnosis in 7 families.

Content Provider	Scilit
Author	Steinberg, Steven J. Elçioglu, Nursel Slade, Christina M. Sankaralingam, Arun Dennis, Nicholas Mohammed, Shehla N. Fensom, Anthony H.
Copyright Year	1999
Description	Journal: American Journal of Medical Genetics
Related Links	https://onlinelibrary.wiley.com/doi/pdf/10.1002/(SICI)1096-8628(19990827)85:5<502::AID-AJMG14>3.0.CO;2-T
Ending Page	510
Page Count	9
Starting Page	502
ISSN	01487299
e-ISSN	10968628
DOI	10.1002/%28sici%291096-8628%2819990827%2985%3A5%3C502%3A%3Aaid-ajmg14%3E3.3.co%3B2-k
Journal	American Journal of Medical Genetics
Issue Number	5
Volume Number	85
Language	English
Publisher	Wiley-Blackwell
Publisher Date	1999-07-14
Access Restriction	Open
Subject Keyword	Journal: American Journal of Medical Genetics Medical Laboratory Technology Zellweger Syndrome Pex Genes Rhizomelic Chondrodysplasia Punctata
Content Type	Text
Resource Type	Article
Subject	Genetics (clinical)

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Peroxisomal disorders: clinical and biochemical studies in 15 children and prenatal diagnosis in 7 families.