Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.

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Bibliographic Details
Title: Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.
Authors: Wieland, I.1, Weidner, C.1, Ciccone, R.2, Lapi, E.3, McDonald-McGinn, D.4, Kress, W.5, Jakubiczka, S.1, Collmann, H.6, Zuffardi, O.2,7, Zackai, E.4, Wieacker, P.1,8 wieacker@uni-muenster.de
Source: Clinical Genetics. Dec2007, Vol. 72 Issue 6, p506-516. 11p. 2 Diagrams, 5 Charts, 1 Graph.
Database: Academic Search Ultimate
Description
ISSN:00099163
DOI:10.1111/j.1399-0004.2007.00905.x