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Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction |
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| Authors: | McCabe Mark J Gaston-Massuet Carles Tziaferi Vaitsa Gregory Louise C Alatzoglou Kyriaki S Signore Massimo Puelles Eduardo Gerrelli Dianne Farooqi I Sadaf Raza Jamal Walker Joanna Kavanaugh Scott I Tsai Pei-San Pitteloud Nelly Martinez-Barbera Juan-Pedro Dattani Mehul T |
| Affiliation: | Clinical and Molecular Genetics Unit, University College London—Institute of Child Health, London WC1N 1EH, United Kingdom. |
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| 本文献已被 PubMed 等数据库收录！ | |