Literature DB >> 8006863

Genetic mechanisms and mental retardation.

R C Trembath1.   

Abstract

The past five years have witnessed rapid and apparently relentless progress in the delineation of the genetic basis of disorders associated with mental retardation. Each gene discovery has a new story to tell but inevitably generates further questions. For the clinical geneticist and, perhaps more importantly, for patients and their families, many of these recent discoveries have yielded information which has immediate implications for diagnostic testing, family and population screening and prenatal testing. Many of the ethical issues consequent upon the rapid progress are only now being addressed. This article highlights a number of disorders whose molecular genetic basis has recently been further characterised. Brain development and maintenance of neurological networks provide the unifying theme; the genetic defects are disparate and each of their mechanisms appears to be novel.

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Year:  1994        PMID: 8006863      PMCID: PMC5400906     

Source DB:  PubMed          Journal:  J R Coll Physicians Lond        ISSN: 0035-8819


  15 in total

1.  Unstable DNA sequence in myotonic dystrophy.

Authors:  H G Harley; S A Rundle; W Reardon; J Myring; S Crow; J D Brook; P S Harper; D J Shaw
Journal:  Lancet       Date:  1992-05-09       Impact factor: 79.321

2.  Epidemiology of tuberous sclerosis.

Authors:  J P Osborne; A Fryer; D Webb
Journal:  Ann N Y Acad Sci       Date:  1991       Impact factor: 5.691

Review 3.  Fragile X mental retardation.

Authors:  R M Winter
Journal:  Arch Dis Child       Date:  1989-09       Impact factor: 3.791

4.  DNA deletion and its parental origin in Angelman syndrome patients.

Authors:  J Hamabe; Y Kuroki; K Imaizumi; T Sugimoto; Y Fukushima; A Yamaguchi; Y Izumikawa; N Niikawa
Journal:  Am J Med Genet       Date:  1991-10-01

5.  Uniparental paternal disomy in Angelman's syndrome.

Authors:  S Malcolm; J Clayton-Smith; M Nichols; S Robb; T Webb; J A Armour; A J Jeffreys; M E Pembrey
Journal:  Lancet       Date:  1991-03-23       Impact factor: 79.321

Review 6.  Dynamic mutations on the move.

Authors:  G R Sutherland; R I Richards
Journal:  J Med Genet       Date:  1993-12       Impact factor: 6.318

7.  Further segregation analysis of the fragile X syndrome with special reference to transmitting males.

Authors:  S L Sherman; P A Jacobs; N E Morton; U Froster-Iskenius; P N Howard-Peebles; K B Nielsen; M W Partington; G R Sutherland; G Turner; M Watson
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

8.  Population screening for fragile X.

Authors:  G Turner; H Robinson; S Laing; M van den Berk; A Colley; A Goddard; S Sherman; M Partington
Journal:  Lancet       Date:  1992-05-16       Impact factor: 79.321

9.  Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy.

Authors:  J Buxton; P Shelbourne; J Davies; C Jones; T Van Tongeren; C Aslanidis; P de Jong; G Jansen; M Anvret; B Riley
Journal:  Nature       Date:  1992-02-06       Impact factor: 49.962

10.  X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis.

Authors:  R J Gibbons; G K Suthers; A O Wilkie; V J Buckle; D R Higgs
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

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  1 in total

1.  Zebrafish homologs of genes within 16p11.2, a genomic region associated with brain disorders, are active during brain development, and include two deletion dosage sensor genes.

Authors:  Alicia Blaker-Lee; Sunny Gupta; Jasmine M McCammon; Gianluca De Rienzo; Hazel Sive
Journal:  Dis Model Mech       Date:  2012-05-01       Impact factor: 5.758

  1 in total

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