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Manitoba aboriginal kindred with original cerebro-oculo-facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene
Journal article   Peer reviewed

Manitoba aboriginal kindred with original cerebro-oculo-facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene

LB Meira, JM Graham, CR Greenberg, DB Busch, ATB Doughty, DW Ziffer, DM Coleman, I Savre-Train and EC Friedberg
AMERICAN JOURNAL OF HUMAN GENETICS, Vol.66(4), pp.1221-1228
01/04/2000
DOI: https://doi.org/10.1086/302867

Abstract

Science & Technology Life Sciences & Biomedicine Genetics & Heredity GENETICS & HEREDITY MENTAL-RETARDATION COFS SYNDROME MARTSOLFS SYNDROME ACTIVE GENES CATARACTS REPAIR INHERITANCE SIBLINGS CELLS ERCC6
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