Maloney, Viv
16  results:
Search for persons X
?
2

A 2.3Mb deletion of 17q24.2–q24.3 associated with 'Carney C..:

Blyth, Moira ; Huang, Shuwen ; Maloney, Viv..
European Journal of Medical Genetics.  51 (2008)  6 - p. 672-678 , 2008
 
?
4

SHOX mutations in a family and a fetus with Langer mesomeli..:

Thomas, N. Simon ; Maloney, Viv ; Bass, Paul...
American Journal of Medical Genetics Part A.  128A (2004)  2 - p. 179-184 , 2004
 
?
5

Incomplete penetrance, variable expressivity, or dosage ins..:

Bateman, Mark S. ; Collinson, Morag N. ; Bunyan, David J....
American Journal of Medical Genetics Part A.  176 (2017)  2 - p. 319-329 , 2017
 
?
6

8p23.1 duplication syndrome; common, confirmed, and novel f..:

Barber, John C.K. ; Rosenfeld, Jill A. ; Foulds, Nicola...
American Journal of Medical Genetics Part A.  161 (2013)  3 - p. 487-500 , 2013
 
?
8

Inverted duplication of 1q32.1 to 1q44 characterized by arr..:

Balasubramanian, Meena ; Barber, John C.K. ; Collinson, Morag N....
American Journal of Medical Genetics Part A.  149A (2009)  4 - p. 793-797 , 2009
 
?
9

Transmitted duplication of 12q21.32–12q22 includes 48 genes..:

Barber, John C.K. ; Maloney, Viv K. ; Kirchhoff, Maria...
American Journal of Medical Genetics Part A.  143A (2007)  6 - p. 615-618 , 2007
 
1-15