Literature DB >> 6469247

Autosomal fragile sites not a current indication for prenatal diagnosis.

F Hecht, B K Hecht.   

Abstract

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Year:  1984        PMID： 6469247     DOI： 10.1007/bf00291370

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


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  5 in total

1.  Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man.

Authors:  R E Magenis; F Hecht; E W Lovrien
Journal:  Science       Date:  1970-10-02       Impact factor: 47.728

2.  Fragile chromosome 16(q22) cause a balanced translocation at the same point.

Authors:  J M García-Sagredo; C San Román; M E Gallego Gómez; G Lledo
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

3.  BrdU-sensitive fragile site on long arm of chromosome 16.

Authors:  G Croci
Journal:  Am J Hum Genet       Date:  1983-05       Impact factor: 11.025

4.  Demonstration of a heritable fragile site in human chromosome 16 with distamycin A.

Authors:  M Schmid; C Klett; A Niederhofer
Journal:  Cytogenet Cell Genet       Date:  1980

5.  DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes.

Authors:  T W Glover; C Berger; J Coyle; B Echo
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
  5 in total
  2 in total

1.  Population cytogenetics of folate-sensitive fragile sites. II. Autosomal rare fragile sites.

Authors:  M Kähkönen; C Tengström; T Alitalo; R Matilainen; M Kaski; E Airaksinen
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

2.  Familial fragile site found at the cancer breakpoint (1)(q32). Inducibility by distamycin A, concomitance with fragile (16)(q22).

Authors:  F Shabtai; J Hart; D Klar; I Halbrecht
Journal:  Hum Genet       Date:  1986-07       Impact factor: 4.132
  2 in total

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