Front & Back Matter.
- Published in:
- Molecular Syndromology, 2019, v. 10, n. 6, p. 1, doi. 10.1159/000506034
- Publication type:
- Article
Works matching IS 16618769 AND DT 2019 AND VI 10 AND IP 6
Results: 11
1
2
A Rare Case of Mosaic Unbalanced Non-Robertsonian Translocation Involving Chromosomes 15 and 22 with Congenital Abnormalities in Monozygotic Twins.
- Published in:
- Molecular Syndromology, 2019, v. 10, n. 6, p. 320, doi. 10.1159/000505004
- By:
- Publication type:
- Article
3
Genes Positively Selected in Domesticated Mammals Are Significantly Dysregulated in the Blood of Individuals with Autism Spectrum Disorders.
- Published in:
- Molecular Syndromology, 2019, v. 10, n. 6, p. 306, doi. 10.1159/000505116
- By:
- Publication type:
- Article
4
Contents Vol. 10, 2019.
- Published in:
- Molecular Syndromology, 2019, v. 10, n. 6, p. I, doi. 10.1159/000505765
- Publication type:
- Article
5
Interstitial 4q Deletion Syndrome Including NR3C2 Causing Pseudohypoaldosteronism.
- Published in:
- Molecular Syndromology, 2019, v. 10, n. 6, p. 327, doi. 10.1159/000505279
- By:
- Publication type:
- Article
6
Novel Ocular and Inner Ear Anomalies in a Patient with Myhre Syndrome.
- Published in:
- Molecular Syndromology, 2019, v. 10, n. 6, p. 339, doi. 10.1159/000504829
- By:
- Publication type:
- Article
7
NUP188 Biallelic Loss of Function May Underlie a New Syndrome: Nucleoporin 188 Insufficiency Syndrome?
- Published in:
- Molecular Syndromology, 2019, v. 10, n. 6, p. 313, doi. 10.1159/000504818
- By:
- Publication type:
- Article
8
Cardiofaciocutaneous Syndrome Phenotype in a Case with de novo KRAS Pathogenic Variant.
- Published in:
- Molecular Syndromology, 2019, v. 10, n. 6, p. 344, doi. 10.1159/000504374
- By:
- Publication type:
- Article
9
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa.
- Published in:
- Molecular Syndromology, 2019, v. 10, n. 6, p. 332, doi. 10.1159/000504210
- By:
- Publication type:
- Article
10
Deep Phenotyping of Development, Communication and Behaviour in Phelan-McDermid Syndrome.
- Published in:
- 2019
- By:
- Publication type:
- Abstract
11
Genomic Earthquakes in the Human Germline and Their Ramifications.
- Published in:
- Molecular Syndromology, 2019, v. 10, n. 6, p. 291, doi. 10.1159/000503366
- By:
- Publication type:
- Article