Literature DB >> 9783718

Molecular evidence that fragile X syndrome occurs in the South African black population.

A Goldman, T Jenkins, A Krause.   

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Year:  1998        PMID: 9783718      PMCID: PMC1051470          DOI: 10.1136/jmg.35.10.878

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


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  8 in total

1.  Fragile X syndrome occurs in the South African black population.

Authors:  A Goldman; A Krause; T Jenkins
Journal:  S Afr Med J       Date:  1997-04

2.  A marker X chromosome associated with nonspecific male mental retardation. The first South African cases.

Authors:  P A Venter; G S Gericke; B Dawson; J Op't Hof
Journal:  S Afr Med J       Date:  1981-11-21

3.  Frequency of Fra X syndrome among institutionalized mentally retarded males in Poland.

Authors:  T Mazurczak; E Bocian; M Milewski; E Obersztyn; H Stańczak; J Bal; K Szamotulska; M W Karwacki
Journal:  Am J Med Genet       Date:  1996-07-12

4.  Fragile X syndrome: incidence, clinical and cytogenetic findings in the black and white populations of South Carolina.

Authors:  C E Schwartz; M C Phelan; L H Pulliam; G Wilkes; L V Vanner; K L Albiez; W A Potts; R C Rogers; R J Schroer; R A Saul
Journal:  Am J Med Genet       Date:  1988 May-Jun

5.  Comparison between the cytogenetic test for fragile X and the molecular analysis of the FMR-1 gene in Japanese mentally retarded individuals.

Authors:  Y Hofstee; T Arinami; H Hamaguchi
Journal:  Am J Med Genet       Date:  1994-07-15

6.  DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 gene.

Authors:  A M van den Ouweland; B B de Vries; P L Bakker; W H Deelen; E de Graaff; J O van Hemel; B A Oostra; M F Niermeijer; D J Halley
Journal:  Am J Med Genet       Date:  1994-07-15

7.  The Martin-Bell syndrome in South Africa.

Authors:  P A Venter; J Op't Hof; D J Coetzee
Journal:  Am J Med Genet       Date:  1986 Jan-Feb

8.  Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

Authors:  F Rousseau; P Rouillard; M L Morel; E W Khandjian; K Morgan
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

  8 in total
  3 in total

Review 1.  Fragile X syndrome: the FMR1 CGG repeat distribution among world populations.

Authors:  Emmanuel Peprah
Journal:  Ann Hum Genet       Date:  2011-12-21       Impact factor: 1.670

Review 2.  FMR1 and the fragile X syndrome: human genome epidemiology review.

Authors:  D C Crawford; J M Acuña; S L Sherman
Journal:  Genet Med       Date:  2001 Sep-Oct       Impact factor: 8.822

Review 3.  Fragile X syndrome in Korea: a case series and a review of the literature.

Authors:  Shin-Young Yim; Bo Hyun Jeon; Jung A Yang; Hyon J Kim
Journal:  J Korean Med Sci       Date:  2008-06       Impact factor: 2.153

  3 in total

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