Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

Author:

Stankiewicz Paweł,Sen Partha,Bhatt Samarth S.,Storer Mekayla,Xia Zhilian,Bejjani Bassem A.,Ou Zhishuo,Wiszniewska Joanna,Driscoll Daniel J.,Bolivar Juan,Bauer Mislen,Zackai Elaine H.,McDonald-McGinn Donna,Nowaczyk Małgorzata M.J.,Murray Mitzi,Shaikh Tamim H.,Martin Vicki,Tyreman Matthew,Simonic Ingrid,Willatt Lionel,Paterson Joan,Mehta Sarju,Rajan Diana,Fitzgerald Tomas,Gribble Susan,Prigmore Elena,Patel Ankita,Shaffer Lisa G.,Carter Nigel P.,Cheung Sau Wai,Langston Claire,Shaw-Smith Charles

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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3. Alveolar capillary dysplasia. Report of a case of prolonged life without extracorporeal membrane oxygenation (ECMO) and review of the literature;Al-Hathlol;Early Hum. Dev.,2000

4. Alveolar capillary dysplasia: a six-year single center experience;Eulmesekian;J. Perinat. Med.,2005

5. Familial persistent pulmonary hypertension of the newborn resulting from misalignment of the pulmonary vessels (congenital alveolar capillary dysplasia);Vassal;J. Med. Genet.,1998

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