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Biotin-sensitive 3-methylcrotonylglycinuria in a patient wit…
Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay%252C ectodermal abnormalities%252C neonatal progeroid appearance%252C and developmental delay.
Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay%252C ectodermal abnormalities%252C neonatal progeroid appearance%252C and developmental delay.
Article, Chapter
Authors: Koene
Publication: Clinical Dysmorphology
Published: Wolters Kluwer Health _ Lippincott Williams and Wilkins
ISSN: 0962-8827
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View Full Text Source:Clinical Dysmorphology,Clinical Dysmorphology,Journals@Ovid Opens in new Window
Journal:  Clinical Dysmorphology Source:Journals@Ovid Opens in new Window
Collection:  Journals@Ovid Opens in new Window
Coverage:
  • 1992-01~present; volume:1~present;issue:1~present
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