Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma-Reference-Cited by-同舟云学术

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Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma

Published:2001-01 Issue:1 Volume:22 Page:35-41
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Finzi Simone,Pinto Carla F.,Wiggs Janey L.

Publisher

Swets & Zeitlinger Publishers

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1076/opge.22.1.35.2234

Reference8 articles.

1. Ocular findings in a 4 p- deletion syndrome (Wolf-Hirschhorn)

2. Peters' Anomaly and Combination with Other Malformations (Series of 16 Patients)

3. Absence of Malignant Hyperthermia in an Infant With Wolf-Hirschhorn Syndrome Undergoing Anesthesia for Ophthalmic Surgery

4. Syndrome of proximal interstitial deletion 4p15: Report of three cases and review of the literature

Cited by 13 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. Severe congenital bilateral corneal ulceration due to Wolf-Hirschhorn syndrome: a case-report and review of the ophthalmic literature;Journal of American Association for Pediatric Ophthalmology and Strabismus;2019-10

2. Congenital cavitary optic disc anomaly and Axenfeld’s anomaly in Wolf-Hirschhorn syndrome: A case report and review of the literature;Ophthalmic Genetics;2017-12-04

3. Síndrome de Wolf-Hirschhorn. Descripción de una cohorte española de 51 casos y revisión de la bibliografía;Revista de Neurología;2017

4. Oculofacial Manifestations of Chromosomal Aberrations;The Eye in Pediatric Systemic Disease;2017

5. Rare Diseases Leading to Childhood Glaucoma: Epidemiology, Pathophysiogenesis, and Management;BioMed Research International;2015

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