Antenatal finding of 16q24.1 duplication including FOXF1, revealing an autosomal dominant familial pathology with congenital short bowel, malrotation and renal abnormalities-Reference-Cited by-同舟云学术

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Antenatal finding of 16q24.1 duplication including FOXF1, revealing an autosomal dominant familial pathology with congenital short bowel, malrotation and renal abnormalities

Published:2021-09 Issue:5 Volume:45 Page:101562
ISSN:2210-7401
Container-title:Clinics and Research in Hepatology and Gastroenterology
language:en
Short-container-title:Clinics and Research in Hepatology and Gastroenterology

Author:

Lavillaureix Alinoë,Foulon Gauthier,Launay Erika,Belaud-Rotureau Marc-Antoine,Thibault Ronan,Lambe Cécile,Aussel Dominique,Pasquier Laurent,Odent Sylvie,Arnaud Alexis^ORCID,Habonimana Edouard,Dabadie Alain,Jaillard Sylvie^ORCID

Funder

Murdoch Children's Research Institute

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference9 articles.

1. Short small intestine associated with malrotation: a newly described congenital cause of intestinal malabsorption;Hamilton;Gastroenterology,1969

2. Congenital Short Bowel Syndrome: from clinical and genetic diagnosis to the molecular mechanisms involved in intestinal elongation;van der Werf;Biochim Biophys Acta BBA - Mol Basis Dis,2015

3. International standing committee on human cytogenomic nomenclature,2016

4. Establishing norms for intestinal length in children;Struijs;J Pediatr Surg,2009

5. Review of genetic factors in intestinal malrotation;Martin;Pediatr Surg Int,2010

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