Complex Compound Inheritance of Lethal Lung Developmental Disorders due to Disruption of the TBX-FGF Pathway.

Journal: American Journal of Human Genetics

Published: 2019-01-02

DOI: 10.1016/j.ajhg.2018.12.010

Affiliations: 64

Authors: 72

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Institutions FC
Service de Génétique Médicale, CHU de Nantes, France 0.08
University Hospital Nantes (CHU de Nantes), France 0.07
Department of Molecular and Human Genetics, BCM, United States of America (USA) 0.07
Institut du Thorax (IdT), France 0.05
Lyon University Hospital (HCL), France 0.04
Seattle Children's Hospital, United States of America (USA) 0.03
Division of Genetic Medicine, UW, United States of America (USA) 0.03
CHU de Bordeaux, France 0.03
Department of Pediatrics, VU, United States of America (USA) 0.03
Centre Hospitalier Universitaire de Lille (CHU Lille), France 0.03
Kaiser Permanente Sacramento Genetics Department, United States of America (USA) 0.03
Baylor Genetics, United States of America (USA) 0.02
Human Genome Sequencing Center (HGSC), BCM, United States of America (USA) 0.02
Texas Children's Hospital, BCM, United States of America (USA) 0.02
Regeneron Genetics Center, United States of America (USA) 0.01
Kaiser Permanente Oakland Medical Center, United States of America (USA) 0.01
Division of Genetics and Genomic Medicine, WUSTL, United States of America (USA) 0.01
Toulouse University Hospital (CHU-Toulouse), France 0.01
Princess Anne Hospital, University Hospital Southampton NHS Foundation Trust, United Kingdom (UK) 0.01
Department of Clinical Genetics, Leiden University, Netherlands 0.01
Assistance Publique-Hopitaux de Marseille (AP-HM), France 0.01
Centre de Génétique Médicale de Marseille (MMG), France 0.01
Department of Medical and Biological Sciences (DSMB), UNIUD, Italy 0.01
Antonio Cardarelli Hospital, Italy 0.01
Department of Pathology and Immunology, BCM, United States of America (USA) 0.01
Rennes University Hospital (CHU Rennes), France 0.01
Department of Pediatrics, UTHSC, United States of America (USA) 0.01
Hôpital de la Conception, France 0.01
Epidermis Differentiation and Rheumatoid Autoimmunity (UDEAR), France 0.01
Akron Children's Hospital, United States of America (USA) 0.01
School of Women's and Children's Health (SPHCM), UNSW, Australia 0.01
Kaiser Permanente Washington, United States of America (USA) 0.01
Phoenix Children's Hospital, United States of America (USA) 0.01
Department of Pathology and Laboratory Medicine, UBC, Canada 0.01
Department of Medical Genetics, UBC, Canada 0.01
Prince of Wales Private Hospital, Australia 0.01
Division of Medical Genetics, UW, United States of America (USA) 0.01
Antoine Beclere Hospital, France 0.01
Centre Hospitalier Universitaire de Caen (CHU), UNICAEN, France 0.01
Department of Clinical Genetics, Rigshospitalet, Denmark 0.01
Department of Cellular and Molecular Medicine (ICMM), UCPH, Denmark 0.01
Department of Genetics and Pharmaceutical Microbiology, PUMS, Poland 0.01
Department of Pediatrics, CU Anschutz, United States of America (USA) 0.01
Children's Hospital Colorado, United States of America (USA) 0.01
School of Medical Sciences (SoMS), UNSW, Australia 0.01
Department of Medical Genetics, NRIMC, Poland 0.01
Department of Pediatrics, CU, United States of America (USA) 0.01
Department of Medicine, CU, United States of America (USA) 0.01
Institute of Computer Science, WUT, Poland 0.01
Sydney Children's Hospital (SCH), Australia 0.01
Department of Clinical Medicine, UCPH, Denmark 0
Sydney Medical School (SMS), USYD, Australia 0
Discipline of Child and Adolescent Health, CHW USYD, Australia 0
National Research Institute of Mother and Child (NRIMC), Poland 0
Kennedy Center, Rigshospitalet, Denmark 0
Children's Hospital at Westmead (CHW), USYD, Australia 0
Department of Molecular Physiology and Biophysics, BCM, United States of America (USA) 0
Department of Pediatrics, BCM, United States of America (USA) 0

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