Inverted Duplication and Deletion of 10q25q26 in a Patient without Any Obvious Skeletal Anomalies.
- Published in:
- Molecular Syndromology, 2012, v. 3, n. 4, p. 185, doi. 10.1159/000343047
- By:
- Publication type:
- Article
Works matching IS 16618769 AND DT 2012 AND VI 3 AND IP 4
Results: 7
1
2
Correction.
- Published in:
- Molecular Syndromology, 2012, v. 3, n. 4, p. 157
- Publication type:
- Article
3
Infrequent Manifestations of Kabuki Syndrome in a Patient with Novel MLL2 Mutation.
- Published in:
- Molecular Syndromology, 2012, v. 3, n. 4, p. 180, doi. 10.1159/000342253
- By:
- Publication type:
- Article
4
Partial Blindness to Submicron Topography in NF1 Haploinsufficient Cultured Fibroblasts Indicates a New Function of Neurofibromin in Regulation of Mechanosensoric.
- Published in:
- Molecular Syndromology, 2012, v. 3, n. 4, p. 169, doi. 10.1159/000342698
- By:
- Publication type:
- Article
5
From the Transcription of Genes Involved in Ectodermal Dysplasias to the Understanding of Associated Dental Anomalies.
- Published in:
- Molecular Syndromology, 2012, v. 3, n. 4, p. 158, doi. 10.1159/000342833
- By:
- Publication type:
- Article
6
LEOPARD Syndrome: Clinical Features and Gene Mutations.
- Published in:
- Molecular Syndromology, 2012, v. 3, n. 4, p. 145, doi. 10.1159/000342251
- By:
- Publication type:
- Article
7
Don't' Mess with RUNX1.
- Published in:
- Molecular Syndromology, 2012, v. 3, n. 4, p. 143, doi. 10.1159/000342878
- By:
- Publication type:
- Article