Congenital Hypothyroidism in Peters Plus Syndrome-Reference-Cited by-同舟云学术

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Congenital Hypothyroidism in Peters Plus Syndrome

Published:2006-01 Issue:2 Volume:27 Page:67-69
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Kosaki Rika,Kamiishi Akiko,Sugiyama Ryusuke,Kawai Masataka,Hasegawa Tomonobu,Kosaki Kenjiro

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1080/13816810600678170

Reference8 articles.

1. Two unrelated children with developmental delay, short stature and anterior chamber cleavage disorder, cerebellar hypoplasia, endocrine disturbances and tracheostenosis

2. A child with sclerocornea, short limbs, short stature, and distinct facial appearance

3. Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly

Cited by 6 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. Phenotypic Spectrum of Peters Anomaly: Implications for Management;Cornea;2021-06-28

2. Congenital hypothyroidism in Rieger Syndrome;Ophthalmic Genetics;2014-03-25

3. The Use of Autozygosity Mapping and Next-Generation Sequencing in Understanding Anterior Segment Defects Caused by an Abnormal Development of the Lens;Human Heredity;2014

4. Familial Peters Plus syndrome with absent anal canal, sacral agenesis and sensorineural hearing loss: Expanding the clinical spectrum;Egyptian Journal of Medical Human Genetics;2013-10

5. Severe peter plus syndrome: A rare case report;International Journal of Medical Research & Health Sciences;2013

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