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- 2005
-
Mark
PTPN11 mutations play a minor role in isolated congenital heart disease
Weismann, Constance G LU
; Hager, A
; Kaemmerer, H
; Maslen, C L
; Morris, Cynthia D
; Schranz, D
; Kreuder, J
and Gelb, B D
(2005)
In American Journal of Medical Genetics. Part A
136A(2).
p.51-146
- Contribution to journal › Article
- 2001
-
Mark
Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation
Zhao, F ; Weismann, C G LU
; Satoda, M
; Pierpont, M E
; Sweeney, E
; Thompson, E M
and Gelb, B D
(2001)
In American Journal of Human Genetics
69(4).
p.695-703
- Contribution to journal › Article