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An exon 1 deletion in OTC identified using chromosomal microarray analysis in a mother and her two affected deceased newborns: Implications for the prenatal diagnosis of ornithine transcarbamylase deficiency

✍ Scribed by Fabiola Quintero-Rivera; Joshua L. Deignan; Jane Peredo; Wayne W. Grody; Barbara Crandall; Maureen Sims; Stephen D. Cederbaum


Book ID
116989062
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
376 KB
Volume
101
Category
Article
ISSN
1096-7192

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