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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

Meira, LB, Graham, JM, Greenberg, CR, Busch, DB, Doughty, ATB, Ziffer, DW, Coleman, DM, Savre-Train, I and Friedberg, EC (2000) Manitoba aboriginal kindred with original cerebro-oculo-facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene AMERICAN JOURNAL OF HUMAN GENETICS, 66 (4). pp. 1221-1228.

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Item Type: Article
Authors :
NameEmailORCID
Meira, LBl.meira@surrey.ac.ukUNSPECIFIED
Graham, JMUNSPECIFIEDUNSPECIFIED
Greenberg, CRUNSPECIFIEDUNSPECIFIED
Busch, DBUNSPECIFIEDUNSPECIFIED
Doughty, ATBUNSPECIFIEDUNSPECIFIED
Ziffer, DWUNSPECIFIEDUNSPECIFIED
Coleman, DMUNSPECIFIEDUNSPECIFIED
Savre-Train, IUNSPECIFIEDUNSPECIFIED
Friedberg, ECUNSPECIFIEDUNSPECIFIED
Date : 1 April 2000
Identification Number : https://doi.org/10.1086/302867
Uncontrolled Keywords : Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, GENETICS & HEREDITY, MENTAL-RETARDATION, COFS SYNDROME, MARTSOLFS SYNDROME, ACTIVE GENES, CATARACTS, REPAIR, INHERITANCE, SIBLINGS, CELLS, ERCC6
Related URLs :
Depositing User : Symplectic Elements
Date Deposited : 17 May 2017 08:53
Last Modified : 17 May 2017 14:38
URI: http://epubs.surrey.ac.uk/id/eprint/821291

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