Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction
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| Description | scientific article |
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author: Sadaf Farooqi Juan Pedro Martinez-Barbera Pei-San Tsai Nelly Pitteloud Mehul T Dattani Carles Gaston-Massuet Eduardo Puelles Dianne Gerrelli |
| Publication date | August 10, 2011 |
| Language | English |
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