Literature DB >> 2224081

The chromosome-breakage syndromes: rare disorders that provide models for studying somatic mutation.

J German1.   

Abstract

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Year:  1990        PMID： 2224081

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  4 in total

1.  RAD51D- and FANCG-dependent base substitution mutagenesis at the ATP1A1 locus in mammalian cells.

Authors:  John M Hinz; Salustra S Urbin; Larry H Thompson
Journal:  Mutat Res       Date:  2009-03-18       Impact factor: 2.433

Review 2.  Cytogenetic analysis in prenatal diagnosis.

Authors:  S A Schonberg
Journal:  West J Med       Date:  1993-09

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

4.  Disparate contributions of the Fanconi anemia pathway and homologous recombination in preventing spontaneous mutagenesis.

Authors:  John M Hinz; Peter B Nham; Salustra S Urbin; Irene M Jones; Larry H Thompson
Journal:  Nucleic Acids Res       Date:  2007-05-21       Impact factor: 16.971
  4 in total

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