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The 9p- deletion syndrome. Report of a patient with a 46, XX, 9p- constitution due to a paternal t(9p-; 15q+) translocation

✍ Scribed by E. Orye; H. Verhaaren; A. M. Van den Bogaert-Van Heesvelde

Book ID: 119838279
Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 526 KB
Volume: 8
Category: Article
ISSN: 0009-9163
DOI: 10.1111/j.1399-0004.1975.tb01513.x

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