Severe coarctation of the aorta, developmental delay, and multiple dysmorphic features in a child with SMAD6 and SMARCA4 variants-Reference-Cited by-同舟云学术

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Severe coarctation of the aorta, developmental delay, and multiple dysmorphic features in a child with SMAD6 and SMARCA4 variants

Published:2022-11 Issue:11 Volume:65 Page:104601
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Caengprasath Natarin^ORCID,Buasong Aayalida,Ittiwut Chupong,Khongphatthanayothin Apichai,Porntaveetus Thantrira^ORCID,Shotelersuk Vorasuk^ORCID

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference13 articles.

1. Endocardial Brg1 disruption illustrates the developmental origins of semilunar valve disease;Akerberg;Dev. Biol.,2015

2. Mental retardation with absent fifth fingernail and terminal phalanx;Coffin;Am. J. Dis. Child.,1970

3. A role for smad6 in development and homeostasis of the cardiovascular system;Galvin;Nat. Genet.,2000

4. Candidate gene resequencing in a large bicuspid aortic valve-associated thoracic aortic aneurysm cohort: SMAD6 as an important contributor;Gillis;Front. Physiol.,2017

5. Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability;Lelieveld;Nat. Neurosci.,2016

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