Front & Back Matter.
- Published in:
- Molecular Syndromology, 2016, v. 6, n. 5, p. X, doi. 10.1159/000444378
- Publication type:
- Article
Works matching IS 16618769 AND DT 2016 AND VI 6 AND IP 5
Results: 9
1
2
Chromothripsis after Stumbling through DNA Replication.
- Published in:
- Molecular Syndromology, 2016, v. 6, n. 5, p. 207, doi. 10.1159/000441081
- By:
- Publication type:
- Article
3
Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors.
- Published in:
- Molecular Syndromology, 2016, v. 6, n. 5, p. 210, doi. 10.1159/000441408
- By:
- Publication type:
- Article
4
Clinical and Genetic Heterogeneity of the 15q13.3 Microdeletion Syndrome.
- Published in:
- Molecular Syndromology, 2016, v. 6, n. 5, p. 222, doi. 10.1159/000443343
- By:
- Publication type:
- Article
5
Jacobsen Syndrome: Surgical Complications due to Unsuspected Diagnosis, the Importance of Molecular Studies in Patients with Craniosynostosis.
- Published in:
- Molecular Syndromology, 2016, v. 6, n. 5, p. 229, doi. 10.1159/000442477
- By:
- Publication type:
- Article
6
Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial Features.
- Published in:
- Molecular Syndromology, 2016, v. 6, n. 5, p. 236, doi. 10.1159/000443232
- By:
- Publication type:
- Article
7
22q11.2 Deletion Syndrome due to a Translocation t(6;22) in a Patient Conceived via in vitro Fertilization.
- Published in:
- Molecular Syndromology, 2016, v. 6, n. 5, p. 242, doi. 10.1159/000441243
- By:
- Publication type:
- Article
8
Pre- and Postnatal Analysis of Chromosome 15q26.1 and 8p23.1 Deletions in Congenital Diaphragmatic Hernia.
- Published in:
- Molecular Syndromology, 2016, v. 6, n. 5, p. 248, doi. 10.1159/000442506
- By:
- Publication type:
- Article
9
A New, Atypical Case of Cobalamin F Disorder Diagnosed by Whole Exome Sequencing.
- Published in:
- Molecular Syndromology, 2016, v. 6, n. 5, p. 254, doi. 10.1159/000441134
- By:
- Publication type:
- Article