Literature DB >> 5054319

X-linked mental retardation and-or hydrocephalus.

K Fried.   

Abstract

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Mesh：

Year:  1972        PMID： 5054319

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  20 in total

1.  Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.

Authors:  L Strain; A F Wright; D T Bonthron
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

2.  MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families.

Authors:  C Schrander-Stumpel; J Fryns; J J Cassiman; E Legius; A Spaepen; C J Höweler
Journal:  J Med Genet       Date:  1992-03       Impact factor: 6.318

3.  Further localization of X-linked hydrocephalus in the chromosomal region Xq28.

Authors:  P J Willems; L Vits; P Raeymaekers; J Beuten; P Coucke; J J Holden; C Van Broeckhoven; S T Warren; M Sagi; D Robinson
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

Review 4.  Non-specific X linked mental retardation.

Authors:  B Kerr; G Turner; J Mulley; A Gedeon; M Partington
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

5.  A modifier locus on chromosome 5 contributes to L1 cell adhesion molecule X-linked hydrocephalus in mice.

Authors:  Alexis Tapanes-Castillo; Eli J Weaver; Robin P Smith; Yoshimasa Kamei; Tamara Caspary; Kara L Hamilton-Nelson; Susan H Slifer; Eden R Martin; John L Bixby; Vance P Lemmon
Journal:  Neurogenetics       Date:  2009-06-30       Impact factor: 2.660

Review 6.  X linked hydrocephalus and MASA syndrome.

Authors:  S Kenwrick; M Jouet; D Donnai
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

7.  Adult fragile X syndrome. Clinico-neuropathologic findings.

Authors:  R D Rudelli; W T Brown; K Wisniewski; E C Jenkins; M Laure-Kamionowska; F Connell; H M Wisniewski
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

Review 8.  Infantile hydrocephalus: a review of epidemiology, classification and causes.

Authors:  Hannah M Tully; William B Dobyns
Journal:  Eur J Med Genet       Date:  2014-06-13       Impact factor: 2.708

9.  X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies.

Authors:  R Bernstein; J Wagner; J Isdale; G T Nurse; A B Lane; T Jenkins
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

10.  The site of a missense mutation in the extracellular Ig or FN domains of L1CAM influences infant mortality and the severity of X linked hydrocephalus.

Authors:  R C Michaelis; Y Z Du; C E Schwartz
Journal:  J Med Genet       Date:  1998-11       Impact factor: 6.318
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