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Next-generation sequencing identifies mutations in Lrp2 as a cause for syndromic craniosynostosis

✍ Scribed by Rachwalski, M.; Li, Y.; Vargel, I.; Mavili, E.; Altmüller, J.; Thiele, H.; Nürnberg, P.; Akarsu, N.; Wollnik, B.

Book ID: 122313757
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 65 KB
Volume: 42
Category: Article
ISSN: 0901-5027
DOI: 10.1016/j.ijom.2013.07.250

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