Study of a possible genetic cause of CHARGE association
CHARGE association, or syndrome as it is now known, is a condition where a number of congenital malformations are non-randomly associated in a recognizable pattern. There are two sets of diagnostic criteria for CHARGE syndrome which are in common usage at present (Blake et al., 1998; Verloes, 2005)....
Main Author: | Johnson, Diana S. |
---|---|
Published: |
University of Glasgow
2010
|
Subjects: | |
Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559892 |
Similar Items
-
Characterisation of anatomical and functional deficits in a mouse model of Rett Syndrome
by: Weng, Shih-Ming
Published: (2012) -
Understanding the pathogenesis of myotonic dystrophy type 1
by: Haworth, Christine
Published: (2008) -
Metabolomic analyses of Drosophila models for human renal disease
by: Hobani, Yahya Hasan
Published: (2012) -
Discovering common genetic variants for hypertension using an extreme case-control strategy
by: Hastie, Claire E.
Published: (2011) -
Genetic association studies of bipolar disorder
by: Bass, Nicholas James
Published: (2008)