Language Impairment Resulting from a de novo Deletion of 7q32.1q33.
- Published in:
- Molecular Syndromology, 2016, v. 7, n. 5, p. 292, doi. 10.1159/000448208
- By:
- Publication type:
- Article
Works matching IS 16618769 AND DT 2016 AND VI 7 AND IP 5
Results: 7
1
2
Distal 7q11.23 Duplication, an Emerging Microduplication Syndrome: A Case Report and Further Characterisation.
- Published in:
- Molecular Syndromology, 2016, v. 7, n. 5, p. 287, doi. 10.1159/000448698
- By:
- Publication type:
- Article
3
PARK2 Microduplication: Clinical and Molecular Characterization of a Further Case and Review of the Literature.
- Published in:
- Molecular Syndromology, 2016, v. 7, n. 5, p. 282, doi. 10.1159/000448852
- By:
- Publication type:
- Article
4
The Family of Crumbs Genes and Human Disease.
- Published in:
- Molecular Syndromology, 2016, v. 7, n. 5, p. 274, doi. 10.1159/000448109
- By:
- Publication type:
- Article
5
Disorders of Transcriptional Regulation: An Emerging Category of Multiple Malformation Syndromes.
- Published in:
- Molecular Syndromology, 2016, v. 7, n. 5, p. 262, doi. 10.1159/000448747
- By:
- Publication type:
- Article
6
Changing Paradigms in Down Syndrome: The First International Conference of the Trisomy 21 Research Society.
- Published in:
- Molecular Syndromology, 2016, v. 7, n. 5, p. 251, doi. 10.1159/000449049
- By:
- Publication type:
- Article
7
When Recessive Genes Mutate to Dominant Gene Action.
- Published in:
- Molecular Syndromology, 2016, v. 7, n. 5, p. 249, doi. 10.1159/000449116
- By:
- Publication type:
- Article