Alveolar Capillary Dysplasia

Haploinsufficiencies ofFOXF1andFOXC2genes associated with lethal alveolar capillary dysplasia and congenital heart disease

(2010) Shihui Yu et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Misplaced pulmonary arteries in an adult patient with pulmonary hypertension

(2010) G B Marshall et al.   BRITISH JOURNAL OF RADIOLOGY

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

(2010) Alexander Hoischen et al.   NATURE GENETICS

Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy

(2010) James R. Lupski et al.   NEW ENGLAND JOURNAL OF MEDICINE

Omphalocele and alveolar capillary dysplasia: A new association

(2010) Luella C. Gerrits et al.   Pediatric Critical Care Medicine

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

(2009) Paweł Stankiewicz et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Exome sequencing identifies the cause of a mendelian disorder

(2009) Sarah B Ng et al.   NATURE GENETICS

Galvanised by a respiratory distress diagnosis

(2008) M E Abdel-Latif et al.   Archives of Disease in Childhood-Education and Practice Edition

Capillary apposition and density in the diagnosis of alveolar capillary dysplasia

(2008) L Melly et al.   HISTOPATHOLOGY

Extracorporeal Membrane Oxygenation for Cardiopulmonary Failure in Pediatric Patients: Is a Second Course Justified?

(2008) Jason C. Fisher et al.   JOURNAL OF SURGICAL RESEARCH

A neonate with coexisting congenital cystic adenomatoid malformation of the lung and alveolar capillary dysplasia: A case report with review of literature

(2008) Peter Paul Roeleveld et al.   Pediatric Critical Care Medicine

Profound hypoxemia and pulmonary hypertension in a 7-month-old infant: Late presentation of alveolar capillary dysplasia

(2008) Sheikh Ahmed et al.   Pediatric Critical Care Medicine