Literature DB >> 8503437

X-linked mental retardation: in pursuit of a gene map.

C E Schwartz.   

Abstract

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Mesh：

Year:  1993        PMID： 8503437      PMCID： PMC1682268     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  57 in total

1.  Familial sex-linked mental retardation.

Authors:  H RENPENNING; J W GERRARD; W A ZALESKI; T TABATA
Journal:  Can Med Assoc J       Date:  1962-11-03       Impact factor: 8.262

2.  XLMR genes: update 1990.

Authors:  G Neri; F Gurrieri; A Gal; H A Lubs
Journal:  Am J Med Genet       Date:  1991 Feb-Mar

Review 3.  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

4.  Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium.

Authors:  G R Sutherland
Journal:  Science       Date:  1977-07-15       Impact factor: 47.728

5.  X-linked mental retardation and-or hydrocephalus.

Authors:  K Fried
Journal:  Clin Genet       Date:  1972       Impact factor: 4.438

6.  X-linked mental retardation, macro-orchidism, and the Xq27 fragile site.

Authors:  G Turner; A Daniel; M Frost
Journal:  J Pediatr       Date:  1980-05       Impact factor: 4.406

7.  X-linked nonspecific mental retardation. Report of a large kindred.

Authors:  K M Yarbrough; P N Howard-Peebles
Journal:  Clin Genet       Date:  1976-02       Impact factor: 4.438

Review 8.  Nomenclature guidelines for X-linked mental retardation.

Authors:  J C Mulley; B Kerr; R Stevenson; H Lubs
Journal:  Am J Med Genet       Date:  1992 Apr 15-May 1

9.  Familial X-linked mental retardation with an X chromosome abnormality.

Authors:  J Harvey; C Judge; S Wiener
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318

10.  Nonspecific X-linked mental retardation II: the frequency in British Columbia.

Authors:  D S Herbst; J R Miller
Journal:  Am J Med Genet       Date:  1980
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  6 in total

1.  X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28.

Authors:  Kimberly A Hahn; Gajja S Salomons; Darci Tackels-Horne; Tim C Wood; Harold A Taylor; Richard J Schroer; Herbert A Lubs; Cornelis Jakobs; Rick L Olson; Kenton R Holden; Roger E Stevenson; Charles E Schwartz
Journal:  Am J Hum Genet       Date:  2002-03-15       Impact factor: 11.025

2.  Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation.

Authors:  R E Stevenson; B Häne; J F Arena; M May; L Lawrence; H A Lubs; C E Schwartz
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

3.  Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21.

Authors:  P A Clark; T Lester; L Villard; M Fontes; C Kinnon
Journal:  J Med Genet       Date:  1994-04       Impact factor: 6.318

4.  Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without alpha-thalassemia.

Authors:  L Villard; A Toutain; A M Lossi; J Gecz; C Houdayer; C Moraine; M Fontès
Journal:  Am J Hum Genet       Date:  1996-03       Impact factor: 11.025

5.  Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).

Authors:  X X Gu; R Decorte; P Marynen; J P Fryns; J J Cassiman; P Raeymaekers
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

6.  Tuber cinereum diverticula in a 28-month-old with xq21 deletion syndrome.

Authors:  Matthew T Whitehead; Gilbert Vezina
Journal:  Case Rep Radiol       Date:  2014-07-13
  6 in total

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