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

J Paediatr Child Health. 2016 Jul;52(7):787-8. doi: 10.1111/jpc.13191.

Dimple Goel^{1

2}, Ju Lee Oei^{1

2}, Antonia W Shand^{2

3}, David Mowat^{2

4}, Christine Loo^{5

6}

¹ Department of Newborn Care, Royal Hospital for Women, Sydney, New South Wales, Australia.
² School of Women's and Children's Health, University of New South Wales, Randwick, New South Wales, Australia.
³ Department of Maternal Fetal Medicine, Royal Hospital for Women, Sydney, New South Wales, Australia.
⁴ Department of Medical Genetics, Sydney Children's Hospital, Sydney, New South Wales, Australia.
⁵ Department of Anatomical Pathology, Prince of Wales Hospital, Sydney, New South Wales, Australia.
⁶ Discipline of Pathology, University of Western Sydney, Sydney, New South Wales, Australia.

No abstract available

Publication types