A distinct dysmorphic syndrome with spinocerebellar ataxia and probable autosomal recessive inheritance-Reference-Cited by-同舟云学术

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A distinct dysmorphic syndrome with spinocerebellar ataxia and probable autosomal recessive inheritance

Published:1985-03 Issue:3 Volume:69 Page:243-245
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

S�nchez-Corona J.,Garc�a-Cruz D.,Gonz�lez-Angulo A.,Alvarez-Arratia M. C.,Rodr�guez R. M.,Cant� J. M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00293033.pdf

Reference7 articles.

1. Boyer SH IV, Chisholm AW, McKusick VA (1962) Cardiac aspect of Friedreich's ataxia. Circulation XXV:493?505

2. Konigsmark BW, Weiner LP (1970) The olivopontocerebellar atrophies: a review. Medicine 49:227?241

3. McKusick VA (1983) Mendelian inheritance in man, 6th edn. Johns Hopkins University Press, Baltimore

4. Pedersen L (1980) Hereditary ataxia in a large Dansh pedigree. Clin Genet 17:385?393

5. Pedersen L, Platz P, Ryder LP, Lamm LU, Dissing J (1980) A linkage study of hereditary ataxias and related disorders. Evidence of heterogeneity of dominant cerebellar ataxia. Hum Genet 54:371?383

Cited by 3 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. Cerebro-facio-articular syndrome of Van Maldergem: confirmation of a new MR/MCA syndrome;Clinical Genetics;2008-06-28

2. Characterization of ataxias with magnetic resonance imaging and spectroscopy;Parkinsonism & Related Disorders;2004-08

3. A catalogue of multiple congenital anomaly syndromes;Multiple Congenital Anomalies;1991

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