Literature DB >> 14189840

[HYPOTHESIS OF CHROMOSOMAL TRANSLOCATION AS A GENETIC INTERPRETATION OF FANCONI'S FAMILIAL CONSTITUTIONAL PANMYELOPATHY].

G FANCONI.   

Abstract

Entities:  

Keywords:  CHILD; CHROMOSOME ABNORMALITIES; CONSANGUINITY; FANCONI SYNDROME; INFANT; TRISOMY

Mesh：

Year:  1964        PMID： 14189840

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN： 0018-022X


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  3 in total

1.  [Hexokinase deficiency in blood cells in a group of kin with familial panmyelopathy (Fanconi type)].

Authors:  G W Löhr; H D Waller; F Anschütz; A Knopp
Journal:  Klin Wochenschr       Date:  1965-08-15

Review 2.  Fanconi anemia: current insights regarding epidemiology, cancer, and DNA repair.

Authors:  Jasmine D Peake; Eishi Noguchi
Journal:  Hum Genet       Date:  2022-05-21       Impact factor: 5.881

Review 3.  Cellular and molecular consequences of defective Fanconi anemia proteins in replication-coupled DNA repair: mechanistic insights.

Authors:  Larry H Thompson; John M Hinz
Journal:  Mutat Res       Date:  2009-02-21       Impact factor: 2.433
  3 in total

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