Found: 3
Select item for more details and to access through your institution.
Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome.
- Published in:
- Human Genetics, 2002, v. 111, n. 4/5, p. 421, doi. 10.1007/s00439-002-0803-6
- By:
- Publication type:
- Article
Deletions in the 3′ Part of the NFIX Gene Including a Recurrent Alu-Mediated Deletion of Exon 6 and 7 Account for Previously Unexplained Cases of Marshall- Smith Syndrome.
- Published in:
- Human Mutation, 2014, v. 35, n. 9, p. 1092, doi. 10.1002/humu.22603
- By:
- Publication type:
- Article
The face in congenital melanocytic nevus syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 5, p. 1014, doi. 10.1002/ajmg.a.34217
- By:
- Publication type:
- Article