Literature DB >> 5901871

Chromosome abnormalities in constitutional aplastic anemia.

G E Bloom, S Warner, P S Gerald, L K Diamond.   

Abstract

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Year:  1966        PMID： 5901871     DOI： 10.1056/NEJM196601062740102

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  35 in total

1.  Fanconi anemia.

Authors:  S Basu; G Garewal; S Kaur; A Trehan; R K Marwaha
Journal:  Indian J Pediatr       Date:  1996 May-Jun       Impact factor: 1.967

2.  [Chromosomal instability in homo- and heterocygocity for microcephalia vera )author's transl)].

Authors:  W Vormittag; E Kunze-Mühl; M Weninger
Journal:  Humangenetik       Date:  1975

3.  Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia.

Authors:  S A Latt; G Stetten; L A Juergens; G R Buchanan; P S Gerald
Journal:  Proc Natl Acad Sci U S A       Date:  1975-10       Impact factor: 11.205

4.  Aplastic anaemia in children. A report of three cases.

Authors:  B R Santhanakrishnan; V S Sridharan; V B Raju
Journal:  Indian J Pediatr       Date:  1976-12       Impact factor: 1.967

5.  Sister chromatid exchange evaluation as an aid to the diagnosis and exclusion of Fanconi's anaemia by induced chromosome damage analysis.

Authors:  R T Howell
Journal:  J Med Genet       Date:  1991-07       Impact factor: 6.318

6.  Acute myelogenous leukaemia in Hurler's syndrome.

Authors:  K T Chen; R W McKenna; R J Desnick
Journal:  J Med Genet       Date:  1978-06       Impact factor: 6.318

7.  Formal genetics of Fanconi's anemia.

Authors:  T M Schroeder; D Tilgen; J Krüger; F Vogel
Journal:  Hum Genet       Date:  1976-06-29       Impact factor: 4.132

8.  Familial thrombocytopenia associated with platelet autoantibodies and chromosome breakage.

Authors:  F M Helmerhorst; D C Heaton; P E Crossen; A E von dem Borne; C P Engelfriet; A T Natarajan
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Prevention of chromosomal breakage in Fanconi's anemia by cocultivation with normal cells.

Authors:  I Nordenson; B Björksten; B Lundh
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

10.  Chromosomal breakage, endomitosis, endoreduplication, and hypersensitivity toward radiomimetric and alkylating agents: a possible new autosomal recessive mutation in a girl with craniosynostosis and microcephaly.

Authors:  N Tommerup; E Mortensen; M H Nielsen; R D Wegner; D Schindler; M Mikkelsen
Journal:  Hum Genet       Date:  1993-10       Impact factor: 4.132
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