Literature DB >> 1757955

Molecular genetics of fragile X: a cytogenetics viewpoint. Report of the Fifth International Symposium on X Linked Mental Retardation, Strasbourg, France, 12 to 16 August 1991 (organiser Dr J-L Mandel).

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Year:  1991        PMID： 1757955      PMCID： PMC1017156          DOI： 10.1136/jmg.28.12.814

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


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  5 in total

1.  Fragile X genotype characterized by an unstable region of DNA.

Authors:  S Yu; M Pritchard; E Kremer; M Lynch; J Nancarrow; E Baker; K Holman; J C Mulley; S T Warren; D Schlessinger
Journal:  Science       Date:  1991-05-24       Impact factor: 47.728

2.  Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.

Authors:  A J Verkerk; M Pieretti; J S Sutcliffe; Y H Fu; D P Kuhl; A Pizzuti; O Reiner; S Richards; M F Victoria; F P Zhang
Journal:  Cell       Date:  1991-05-31       Impact factor: 41.582

3.  Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis.

Authors:  A Vincent; D Heitz; C Petit; C Kretz; I Oberlé; J L Mandel
Journal:  Nature       Date:  1991-02-14       Impact factor: 49.962

4.  Genotype prediction in the fragile X syndrome.

Authors:  M C Hirst; Y Nakahori; S J Knight; C Schwartz; S N Thibodeau; A Roche; T J Flint; J M Connor; J P Fryns; K E Davies
Journal:  J Med Genet       Date:  1991-12       Impact factor: 6.318

5.  Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome.

Authors:  M V Bell; M C Hirst; Y Nakahori; R N MacKinnon; A Roche; T J Flint; P A Jacobs; N Tommerup; L Tranebjaerg; U Froster-Iskenius
Journal:  Cell       Date:  1991-02-22       Impact factor: 41.582
  5 in total

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