X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28.-Reference-Cited by-同舟云学术

X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28.

Published:1991-06-01 Issue:6 Volume:28 Page:429-431
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Fryns J P,Spaepen A,Cassiman J J,van den Berghe H

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference12 articles.

1. Mendelian inheritance in man;McKusick, V.A.,1988

2. The hereditary ataxias and related disorders;Harding, A.E.,1987

3. Linkage studies with the gene for X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2);Sutherland, G.R.; Gedeon, A.K.; Haan, E.A.;Am J Med Genet,1988

4. The MASA syndrome: a new heritable mental retardation syndrome;Blanchine, J.W.; RC, Jr, Lewis;Clin Genet,1974

5. X-linked mental retardation associated with bilateral clasp thumbs anomaly;Gareis, F.; Mason, J.D.;Am J Med Genet,1984

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