Literature DB >> 4436596

The genetic defect in the de Sanctis-Cacchione syndrome.

V M Der Kaloustian, E A de Weerd-Kastelein EA+DEWEERDAAKATELEIN, W J Kleijer, W Keijzer, D Bootsma.   

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Year:  1974        PMID： 4436596     DOI： 10.1111/1523-1747.ep12676556

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN： 0022-202X            Impact factor:   8.551


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  3 in total

1.  Semidominance of rad18-2 for several phenotypic characters in Saccharomyces cerevisiae.

Authors:  V W Mayer; C J Goin
Journal:  Genetics       Date:  1984-04       Impact factor: 4.562

2.  Congenital malformations and developmental disabilities in ataxia-telangiectasia, Fanconi anemia, and xeroderma pigmentosum families.

Authors:  K Welshimer; M Swift
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

3.  Repair protein persistence at DNA lesions characterizes XPF defect with Cockayne syndrome features.

Authors:  Mariangela Sabatella; Arjan F Theil; Cristina Ribeiro-Silva; Jana Slyskova; Karen Thijssen; Chantal Voskamp; Hannes Lans; Wim Vermeulen
Journal:  Nucleic Acids Res       Date:  2018-10-12       Impact factor: 16.971
  3 in total

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