Bilateral anterior segment dysgenesis and persistent fetal vasculature associated with terminal 10q26 deletion-Reference-Cited by-同舟云学术

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Bilateral anterior segment dysgenesis and persistent fetal vasculature associated with terminal 10q26 deletion

Published:2021-10 Issue:5 Volume:25 Page:309-311
ISSN:1091-8531
Container-title:Journal of American Association for Pediatric Ophthalmology and Strabismus
language:en
Short-container-title:Journal of American Association for Pediatric Ophthalmology and Strabismus

Author:

Yang Jessica F.,Roohipourmoallai Ramak,Straughn Penny E.,Sherwood Mark B.,Agarwal-Sinha Swati,Zori Roberto T.,Iyer Siva S.R.

Funder

Research to Prevent Blindness

Publisher

Elsevier BV

Subject

Ophthalmology,Pediatrics, Perinatology, and Child Health

Reference7 articles.

1. Chromosome 10q deletion del (10)(q26.1q26.3) is associated with cataract;Chang;Pediatr Neonatol,2013

2. Terminal deletion of the long arm of chromosome 10;Scigliano;Clin Genet,2004

3. Hearing loss, coloboma and left ventricular enlargement in a boy with an interstitial 10q26 deletion;Ramos;Am J Med Genet C Semin Med Genet,2016

4. A subterminal deletion of the long arm of chromosome 10: a clinical report and review;Courtens;Am J Med Genet A,2006

5. Chromosome 10q26 deletion syndrome: two new cases and a review of the literature;Lin;Mol Med Rep,2016

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