Works matching IS 16618769 AND DT 2013 AND VI 4 AND IP 5
Results: 7
Front & Back Matter.
- Published in:
- Molecular Syndromology, 2013, v. 4, n. 5, p. X, doi. 10.1159/000353922
- Publication type:
- Article
From Single Locus Mendelian Syndromes to Multilocus Genetic-Epigenetic Networks in Human Genetics.
- Published in:
- Molecular Syndromology, 2013, v. 4, n. 5, p. 211, doi. 10.1159/000350003
- By:
- Publication type:
- Article
Towards Identification of Individual Etiologies by Resolving Genomic and Biological Conundrums in Patients with Autism Spectrum Disorders.
- Published in:
- Molecular Syndromology, 2013, v. 4, n. 5, p. 213, doi. 10.1159/000350041
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- Publication type:
- Article
Noonan Syndrome: Comparing Mutation-Positive with Mutation-Negative Dutch Patients.
- Published in:
- Molecular Syndromology, 2013, v. 4, n. 5, p. 227, doi. 10.1159/000350686
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- Publication type:
- Article
More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often Anticipated.
- Published in:
- Molecular Syndromology, 2013, v. 4, n. 5, p. 235, doi. 10.1159/000351127
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- Publication type:
- Article
Haploinsufficiency of ANKRD11 (16q24.3) Is Not Obligatorily Associated with Cognitive Impairment but Shows a Clinical Overlap with Silver-Russell Syndrome.
- Published in:
- Molecular Syndromology, 2013, v. 4, n. 5, p. 246, doi. 10.1159/000351765
- By:
- Publication type:
- Article
De novo 15.5-Mb Interstitial Deletion in 5p in a Male Ascertained by Oligospermia.
- Published in:
- Molecular Syndromology, 2013, v. 4, n. 5, p. 250, doi. 10.1159/000351656
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- Publication type:
- Article