Front & Back Matter.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 4, p. X, doi. 10.1159/000441907
- Publication type:
- Article
Works matching IS 16618769 AND DT 2015 AND VI 6 AND IP 4
Results: 9
1
2
To NIPT or Not to NIPT.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 4, p. 153, doi. 10.1159/000439237
- By:
- Publication type:
- Article
3
A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing Impairment.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 4, p. 156, doi. 10.1159/000439576
- By:
- Publication type:
- Article
4
Clinical and Molecular Characterization of Osteogenesis Imperfecta Type V.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 4, p. 164, doi. 10.1159/000439506
- By:
- Publication type:
- Article
5
Novel KIF7 Mutation in a Tunisian Boy with Acrocallosal Syndrome: Case Report and Review of the Literature.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 4, p. 173, doi. 10.1159/000439414
- By:
- Publication type:
- Article
6
The PHF6 Mutation c.1A>G; pM1V Causes Börjeson-Forsman-Lehmann Syndrome in a Family with Four Affected Young Boys.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 4, p. 181, doi. 10.1159/000441047
- By:
- Publication type:
- Article
7
Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 4, p. 187, doi. 10.1159/000440659
- By:
- Publication type:
- Article
8
Cytogenetic and Molecular Findings in Children with Acute Lymphoblastic Leukemia: Experience of a Single Institution in Argentina.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 4, p. 193, doi. 10.1159/000441046
- By:
- Publication type:
- Article
9
Mitochondrial Dysfunction in a Patient with 8q21.11 Deletion and Charcot-Marie-Tooth Disease Type 2K due to GDAP1 Haploinsufficiency.
- Published in:
- Molecular Syndromology, 2015, v. 6, n. 4, p. 204, doi. 10.1159/000440660
- By:
- Publication type:
- Article