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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
Fabiola Quintero-Rivera, Joshua L. Deignan, Jane Peredo, Wayne W. Grody, Barbara Crandall, Maureen Sims, Stephen D. CederbaumVolume:
101
Year:
2010
Language:
english
DOI:
10.1016/j.ymgme.2010.08.008
File:
PDF, 376 KB
english, 2010