FOXF1 gene mutation in alveolar capillary...

Journal of Paediatrics and Child Health 2016 / 07 Vol. 52; Iss. 7

FOXF1 gene mutation in alveolar capillary dysplasia associated with Hirschsprung's disease and clinical review

Goel, Dimple, Oei, Ju Lee, Shand, Antonia W, Mowat, David, Loo, Christine
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Volume:
52
Language:
english
Journal:
Journal of Paediatrics and Child Health
DOI:
10.1111/jpc.13191
Date:
July, 2016
File:
PDF, 145 KB
english, 2016
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