Literature DB >> 2358299

Recombination and the fragile X.

G K Suthers, G R Sutherland.   

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Year:  1990        PMID： 2358299     DOI： 10.1007/bf00276345

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  6 in total

1.  DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity.

Authors:  W T Brown; A C Gross; C B Chan; E C Jenkins
Journal:  Am J Med Genet       Date:  1986 Jan-Feb

2.  The role of recombination in the evolvement of the fragile X mutation.

Authors:  T Schaap
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

3.  Report of the committee on the genetic constitution of the X and Y chromosomes.

Authors:  K E Davies; J L Mandel; J Weissenbach; M Fellous
Journal:  Cytogenet Cell Genet       Date:  1987

4.  Analysis of linkage relationships between genetic markers around the fragile X locus with special reference to the daughters of normal transmitting males.

Authors:  R M Winter; M E Pembrey
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

5.  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

6.  Further evidence for genetic heterogeneity in the fragile X syndrome.

Authors:  W T Brown; E C Jenkins; A C Gross; C B Chan; M S Krawczun; C J Duncan; S L Sklower; G S Fisch
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132
  6 in total

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