Autosomal recessive Peters anomaly, typical facial appearance, failure to thrive, hydrocephalus, and other anomalies: Further delineation of the Krause-Kivlin syndrome-Reference-Cited by-同舟云学术

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Autosomal recessive Peters anomaly, typical facial appearance, failure to thrive, hydrocephalus, and other anomalies: Further delineation of the Krause-Kivlin syndrome

Published:1991-07-01 Issue:1 Volume:40 Page:34-40
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Frydman Moshe,Weinstock Arie L.,Cohen Herman A.,Savir Hanna,Varsano Itzhak

Publisher

Wiley

Subject

Genetics (clinical)

Reference28 articles.

1. (1969): “Dysgenesis Mesodermalis of the Iris and the Cornea.” Springfield, Ill: Charles C Thomas Publisher.

2. Classification of Corneal Endothelial Disorders Based on Neural Crest Origin

3. Peters’ Anomaly Associated With Partial Deletion of the Long Arm of Chromosome 11

4. UNILATERAL MICROPHTHALMIA WITH CONGENITAL ANTERIOR SYNECHIAE AND SYNDACTYLY

Cited by 31 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. Peters anomaly: An overview;Taiwan Journal of Ophthalmology;2023

2. Glaucoma Syndromes: Insights into Glaucoma Genetics and Pathogenesis from Monogenic Syndromic Disorders;Genes;2021-09-11

3. Peter plus syndrome: A neurosurgeon’s perspective;Journal of Pediatric Neurosciences;2019

4. Peters Anomaly in Twins: A Case Report of a Rare Incident with Novel Comorbidities;Case Reports in Ophthalmology;2016-10-10

5. 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

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