 | Up a level |
Group by: Item Type | No Grouping
Jump to: Journal Article
Number of items: 1.
Journal Article
Pohl, Esther, Aykut, Ayca, Beleggia, Filippo, Karaca, Emin, Durmaz, Burak, Keupp, Katharina, Arslan, Esra, Palamar, Melis 
ORCID: 0000-0002-2494-0131, Yigit, Goekhan, Ozkinay, Ferda and Wollnik, Bernd
(2013).
A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome (vol 132, pg 1311, 2013).
Hum. Genet., 132 (11).
S. 1321 - 1322.
NEW YORK:
SPRINGER.
ISSN 1432-1203