SHANK Mutations May Disorder Brain Development.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 1, p. 1, doi. 10.1159/000368949
- By:
- Publication type:
- Article
Works matching IS 16618769 AND DT 2015 AND VI 6 AND IP 1
Results: 9
1
2
Genomic Sequencing and the Impact of Molecular Diagnosis on Patient Care.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 1, p. 4, doi. 10.1159/000371398
- By:
- Publication type:
- Article
3
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 1, p. 7, doi. 10.1159/000371594
- By:
- Publication type:
- Article
4
Front & Back Matter.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 1, p. X, doi. 10.1159/000380995
- Publication type:
- Article
5
Whole-Exome Sequencing in the Clinic: Lessons from Six Consecutive Cases from the Clinician's Perspective.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 1, p. 23, doi. 10.1159/000371598
- By:
- Publication type:
- Article
6
Clinical and Molecular Heterogeneity in Brazilian Patients with Sotos Syndrome.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 1, p. 32, doi. 10.1159/000370169
- By:
- Publication type:
- Article
7
Cleft Lip/Palate, Short Stature, and Developmental Delay in a Boy with a 5.6-Mb Interstitial Deletion Involving 10p15.3p14.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 1, p. 39, doi. 10.1159/000371404
- By:
- Publication type:
- Article
8
A Novel Mutation in the Endothelin B Receptor Gene in a Moroccan Family with Shah-Waardenburg Syndrome.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 1, p. 44, doi. 10.1159/000371590
- By:
- Publication type:
- Article
9
A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 1, p. 50, doi. 10.1159/000370337
- By:
- Publication type:
- Article