Two brothers with the Marden-Walker syndrome: case report and review-Reference-Cited by-同舟云学术

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Two brothers with the Marden-Walker syndrome: case report and review

Published:1981-02-01 Issue:1 Volume:18 Page:50-53
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Howard F. M,Rowlandson P.

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference11 articles.

1. A new generalised connective tissue syndrome;Marden, P.M.; Walker, W.A.;Am J Dis Chiltd,1966

2. Congenital blepharophimosis associated with a unique generalised myopathy;Schwartz 0, Jampel RS;Arch Ophthalmol

3. Amyoplasia congenita causing malpresentation of the fetus;Ealing, M.I.;J Obst Gynaecol British Enipire,1944

4. Year book of pediatrics;Gellis, S.S.,1963

5. Marden-Walker syndrome;Passarge, E.;Birth De.fects,1975

Cited by 24 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. Kaufman oculocerebrofacial syndrome in sisters with novel compound heterozygous mutation inUBE3B;American Journal of Medical Genetics Part A;2015-02-18

2. THE MARDEN-WALKER SYNDROME: A CASE REPORT AND REVIEW OF THE LITERATURE;Journal of Intellectual Disability Research;2008-06-28

3. Marden-Walker syndrome: case report, literature review and nosologic discussion;Clinical Genetics;2008-04-23

4. Marden-Walker syndrome with some additional anomalies;Pediatrics International;2005-02

5. van den Ende–Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures: Clinical delineation and recurrence in brothers;American Journal of Medical Genetics;2003-04-30

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