A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies

Author:

van de Putte Romy,Dworschak Gabriel C.,Brosens Erwin,Reutter Heiko M.,Marcelis Carlo L. M.,Acuna-Hidalgo Rocio,Kurtas Nehir E.,Steehouwer Marloes,Dunwoodie Sally L.,Schmiedeke Eberhard,Märzheuser Stefanie,Schwarzer Nicole,Brooks Alice S.,de Klein Annelies,Sloots Cornelius E. J.,Tibboel Dick,Brisighelli Giulia,Morandi Anna,Bedeschi Maria F.,Bates Michael D.,Levitt Marc A.,Peña Alberto,de Blaauw Ivo,Roeleveld Nel,Brunner Han G.,van Rooij Iris A. L. M.,Hoischen Alexander

Funder

Radboud Universitair Medisch Centrum

Stichting Vrienden van het Sophia

Deutsche Forschungsgemeinschaft

Publisher

Frontiers Media SA

Subject

Pediatrics, Perinatology, and Child Health

Reference48 articles.

1. Clinical geneticists' views of VACTERL/VATER association;Solomon;Am J Med Genet A.,2012

2. Prevalence Tables - Full member registries from 2011 - 20172019

3. A population study of the VACTERL association: evidence for its etiologic heterogeneity;Khoury;Pediatrics.,1983

4. The spectrum of congenital anomalies of the VATER association: an international study;Botto;Am J Med Genet.,1997

5. VACTERL as primary, polytopic developmental field defects;Martinez-Frias;Am J Med Genet.,1999

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