(Q28236792)
Statements
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2 (English)
0 references
March 2005
0 references
37
0 references
3
0 references
275-81
0 references
1 reference
1 reference
1 reference
1 reference