A distinct dysmorphic syndrome with congenital glaucoma and probable autosomal recessive inheritance-Reference-Cited by-同舟云学术

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A distinct dysmorphic syndrome with congenital glaucoma and probable autosomal recessive inheritance

Published:1990-01 Issue:1 Volume:11 Page:35-40
ISSN:0167-6784
Container-title:Ophthalmic Paediatrics and Genetics
language:en
Short-container-title:Ophthalmic Paediatrics and Genetics

Author:

García-Cruz D.,Mendoza R.,Villar V.,Sanchez-Corona J.,García-Cruz M. O.,Rojas Q.,Chavez-Anaya F.,Nazara Z.,Barrios M. T.,Cantu J. M.

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.3109/13816819009012947

Reference8 articles.

1. Familial hypoplasia of the iris stroma associated with glaucoma.

2. Autosomal dominant iridogoniodysgenesis with associated somatic anomalies: four-generation family with Rieger's syndrome.

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Iridogoniodysgenesis (IGD) and Skeletal Anomalies;Genetic Syndromes;2024

2. Primary congenital glaucoma surgery: outcomes and visual function;International Ophthalmology;2021-07-23

3. A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia;American Journal of Medical Genetics Part A;2010-12-10

4. Epiphyseal dysplasia and other skeletal anomalies in a patient with the 6p25 microdeletion syndrome;American Journal of Medical Genetics Part A;2006

5. Familial iridogoniodysgenesis and skeletal anomalies: a probable new autosomal recessive disorder;Clinical Genetics;2004-05-05

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