Cataracts as a marker of genetic heterogeneity in chondrodysplasia punctata-Reference-Cited by-同舟云学术

Cataracts as a marker of genetic heterogeneity in chondrodysplasia punctata

Published:2008-04-23 Issue:1 Volume:19 Page:64-66
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Happle Rudolf

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1981.tb00669.x/fullpdf

Reference15 articles.

1. Atteintes oculaires des chondrodys-plasies ponctuées. A propos de deux cas;Aron;Arch. Ophtal, (Paris),1977

2. Chondrodysplasia punctata: Is maternal warfarin therapy a factor?;Becker;Amer. J. Dis. Child.,1975

3. Vorzeitiges Auftreten von Knochen- und eigenartigen Verkalkungskernen bei Chondrodysplasia fötalis hypoplasia. Histologische und Röntgenuntersuchungen;Conradi;Jb. Kinderheilk.,1914

4. Follicular atrophoderma and pseudopelade associated with chondrodystrophia calcificans congenita;Curth;J. Invest. Derm.,1949

5. A hereditary factor in chondrodystrophia calcificans congenita;Fraser;New Engl. J. Med.,1954

Cited by 49 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. Osseous and Musculoskeletal Disorders;Albert and Jakobiec's Principles and Practice of Ophthalmology;2022

2. Osseous and Musculoskeletal Disorders;Albert and Jakobiec's Principles and Practice of Ophthalmology;2021

3. Gender and Genodermatoses;Gender and Dermatology;2018

4. Concurrent Chondrodysplasia Punctata Type 2 (Conradi-Hunermann-Happle Syndrome) and Ichthyosis Vulgaris in Teenaged Twin Girls;Pediatric Dermatology;2017-07-21

5. Ocular Manifestations of Systemic Syndromes;The Eye in Pediatric Systemic Disease;2017