Literature DB >> 453205

The importance of being a fragile site.

F Hecht, B Kaiser-McCaw.   

Abstract

Mesh:

Year:  1979        PMID: 453205      PMCID: PMC1685771     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


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  11 in total

1.  Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium.

Authors:  G R Sutherland
Journal:  Science       Date:  1977-07-15       Impact factor: 47.728

2.  Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

3.  Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

4.  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

5.  A marker X chromosome.

Authors:  H A Lubs
Journal:  Am J Hum Genet       Date:  1969-05       Impact factor: 11.025

6.  Persisting clone of cells with an abnormal chromosome in a woman previously irradiated.

Authors:  A Dekaban
Journal:  J Nucl Med       Date:  1965-10       Impact factor: 10.057

7.  Lateral asymmetry in human constitutive heterochromatin: frequency and inheritance.

Authors:  R R Angell; P A Jacobs
Journal:  Am J Hum Genet       Date:  1978-03       Impact factor: 11.025

8.  Constitutional chromosomal breakage.

Authors:  F Giraud; S Ayme; J F Mattei; M G Mattei
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

9.  Giemsa-11 staining of chromosome 1: a newly described heteromorphism.

Authors:  R E Maegenis; T A Donlon; H E Wyandt
Journal:  Science       Date:  1978-10-06       Impact factor: 47.728

10.  Familial X-linked mental retardation with an X chromosome abnormality.

Authors:  J Harvey; C Judge; S Wiener
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318

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  9 in total

1.  Lymphocyte abnormalities in Behçet's syndrome.

Authors:  A M Denman; P J Fialkow; B K Pelton; A C Salo; D J Appleford; C Gilchrist
Journal:  Clin Exp Immunol       Date:  1980-10       Impact factor: 4.330

2.  Inducing fragile sites to express themselves.

Authors:  F Hecht; B Kaiser-McCaw
Journal:  Am J Hum Genet       Date:  1980-07       Impact factor: 11.025

Review 3.  Nonspecific X-linked mental retardation--a review.

Authors:  G Tariverdian; B Weck
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

4.  Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiency.

Authors:  J P Fryns; M Azou; J Jaeken; E Eggermont; J C Pedersen; H Van den Berghe
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

5.  Heritable fragile sites and lymphocyte culture medium containing BrdU.

Authors:  J M Scheres; T W Hustinx
Journal:  Am J Hum Genet       Date:  1980-07       Impact factor: 11.025

6.  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

7.  The use of distamycin A in human lymphocyte cultures.

Authors:  M Schmid; D A Hungerford; A Poppen; W Engel
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Activity of the fragile X in heterozygous carriers.

Authors:  I A Uchida; E M Joyce
Journal:  Am J Hum Genet       Date:  1982-03       Impact factor: 11.025

9.  Heritable fragile sites on human chromosomes. V. A new class of fragile site requiring BrdU for expression.

Authors:  G R Sutherland; E Baker; R S Seshadri
Journal:  Am J Hum Genet       Date:  1980-07       Impact factor: 11.025

  9 in total

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