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Opitz “C” trigonocephaly-like syndrome in a patient with terminal deletion of 2p and partial duplication of 17q

✍ Scribed by Márta Czakó; Mariluce Riegel; Éva Morava; Katalin Bajnóczky; György Kosztolányi

Publisher: John Wiley and Sons
Year: 2004
Tongue: English
Weight: 115 KB
Volume: 131A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.30249

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