Literature DB >> 6109088

Chromosome banding required for studies on X-linked mental retardation.

M A Leversha, G C Webb, S M Pavey.   

Abstract

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Year:  1981        PMID： 6109088     DOI： 10.1016/s0140-6736(81)90160-4

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  10 in total

1.  Deleted X chromosomes in patients with the fragile X syndrome.

Authors:  M Fitchett; M Seabright
Journal:  J Med Genet       Date:  1984-10       Impact factor: 6.318

Review 2.  X-linked mental retardation.

Authors:  C Berry
Journal:  Arch Dis Child       Date:  1981-06       Impact factor: 3.791

Review 3.  The fragile X syndrome: the patients and their chromosomes.

Authors:  M A De Arce; A Kearns
Journal:  J Med Genet       Date:  1984-04       Impact factor: 6.318

4.  Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation.

Authors:  G C Webb; J L Halliday; D B Pitt; C G Judge; M Leversha
Journal:  J Med Genet       Date:  1982-02       Impact factor: 6.318

5.  Chromosomal breakage in normal and fragile X subjects using low folate culture conditions.

Authors:  M Vekemans; B Popovich; D Rosenblatt; P Monroe
Journal:  J Med Genet       Date:  1983-12       Impact factor: 6.318

6.  Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site.

Authors:  P Szabo; M Purrello; M Rocchi; N Archidiacono; B Alhadeff; G Filippi; D Toniolo; G Martini; L Luzzatto; M Siniscalco
Journal:  Proc Natl Acad Sci U S A       Date:  1984-12       Impact factor: 11.205

7.  Further delineation of X-linked mental retardation.

Authors:  D S Herbst; H G Dunn; F J Dill; D K Kalousek; L W Krywaniuk
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

8.  Human chromosome hot points. IV. Uridine-induced hot-point breaks at 3p14 and 16q23-24 and increased expression of fragile site Xq27 in folate-free medium.

Authors:  N Li; X T Zhou
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

9.  FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage.

Authors:  Kim Debacker; Birgitta Winnepenninckx; Neta Ben-Porat; David FitzPatrick; Rob Van Luijk; Stefaan Scheers; Batsheva Kerem; R Frank Kooy
Journal:  J Med Genet       Date:  2007-05       Impact factor: 6.318

10.  The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.

Authors:  M Purrello; B Alhadeff; D Esposito; P Szabo; M Rocchi; M Truett; F Masiarz; M Siniscalco
Journal:  EMBO J       Date:  1985-03       Impact factor: 11.598
  10 in total

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