First Reported Patient with Human ERCC1 Deficiency Has Cerebro-Oculo-Facio-Skeletal Syndrome with a Mild Defect in Nucleotide Excision Repair and Severe Developmental Failure-Reference-Cited by-同舟云学术

First Reported Patient with Human ERCC1 Deficiency Has Cerebro-Oculo-Facio-Skeletal Syndrome with a Mild Defect in Nucleotide Excision Repair and Severe Developmental Failure

Published:2007-03 Issue:3 Volume:80 Page:457-466
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Jaspers Nicolaas G.J.,Raams Anja,Silengo Margherita Cirillo,Wijgers Nils,Niedernhofer Laura J.,Robinson Andria Rasile,Giglia-Mari Giuseppina,Hoogstraten Deborah,Kleijer Wim J.,Hoeijmakers Jan H.J.,Vermeulen Wim

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference57 articles.

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