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- 2005
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Mark
Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith-Magenis syndrome minimum deletion to similar to 650 kb
Schoumans, J ; Staaf, Johan LU
; Jönsson, Göran B
LU
; Rantala, J
; Zimmer, K S
; Borg, Åke
LU
; Nordenskjold, M
and Anderlid, B M
(2005)
In European Journal of Medical Genetics
48(3).
p.290-300
- Contribution to journal › Article