Biallelic ITGB4 variants in familial pyloric atresia without epidermolysis bullosa: Report of two families with five siblings-Reference-Cited by-同舟云学术

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Biallelic ITGB4 variants in familial pyloric atresia without epidermolysis bullosa: Report of two families with five siblings

Published:2021-08-17 Issue:11 Volume:185 Page:3427-3432
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Soyer Tutku¹^ORCID,Karaosmanoglu Beren²^ORCID,Taskiran Ekim Z.²^ORCID,Kiper Pelin Özlem Şimşek³,Karnak İbrahim¹,Boduroğlu Koray³,Utine Gülen Eda³

Affiliation:

1. Department of Pediatric Surgery Hacettepe University, Faculty of Medicine Ankara Turkey

2. Department of Medical Genetics Hacettepe University, Faculty of Medicine Ankara Turkey

3. Department of Pediatric Genetics Hacettepe University, Faculty of Medicine Ankara Turkey

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62462

Reference23 articles.

1. Congenital pyloric atresia: The spectrum;Al‐Salem A.;International Surgery,2002

2. Congenital pyloric atresia, presentation, management, and outcome: A report of 20 cases

3. Pyloric atresia. A hereditary congenital anomaly with autosomal recessive transmission.

4. Congenital pyloric atresia: A report of three cases and a review of the literature;Bronsther B.;Surgery,1971

5. A new prenatal sonographic sign of epidermolysis bullosa

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