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Contents Vol. 6, 2015.
Published in:
Molecular Syndromology, 2016, v. 6, n. 6, p. I, doi. 10.1159/000444613
Publication type:
Article
Front & Back Matter.
Published in:
Molecular Syndromology, 2016, v. 6, n. 6, p. X, doi. 10.1159/000444897
Publication type:
Article
From Telomere Crisis via Dicentric Chromosomes to Kataegis and Chromothripsis.
Published in:
Molecular Syndromology, 2016, v. 6, n. 6, p. 259, doi. 10.1159/000443805
By:
- Poot, Martin
Publication type:
Article
RE(ACT) Congress 9-12 March 2016, Barcelona. 3rd International Congress on Research of Rare and Orphan Diseases. 9th to 12th March 2016. Crowne Plaza Barcelona - Fira Center, Barcelona, Spain: Abstracts.
Published in:
Molecular Syndromology, 2016, v. 6, n. 6, p. 304, doi. 10.1159/000444288
Publication type:
Article
Involvement of Fibroblast Growth Factors and Their Receptors in Epididymo-Testicular Descent and Maldescent.
Published in:
Molecular Syndromology, 2016, v. 6, n. 6, p. 261, doi. 10.1159/000444033
By:
- Hadziselimovic, Faruk
Publication type:
Article
Genomic Alterations Are Enhanced in Placentas from Pregnancies with Fetal Growth Restriction and Preeclampsia: Preliminary Results.
Published in:
Molecular Syndromology, 2016, v. 6, n. 6, p. 276, doi. 10.1159/000444064
By:
- Biron-Shental, Tal;
- Sharony, Reuven;
- Shtorch-Asor, Atalia;
- Keiser, Meirav;
- Sadeh-Mestechkin, Dana;
- Laish, Ido;
- Amiel, Aliza
Publication type:
Article
Neonatal Marfan Syndrome: Report of a Case with an Inherited Splicing Mutation outside the Neonatal Domain.
Published in:
Molecular Syndromology, 2016, v. 6, n. 6, p. 281, doi. 10.1159/000443867
By:
- Le Gloan, Laurianne;
- Hauet, Quentin;
- David, Albert;
- Hanna, Nadine;
- Arfeuille, Chloé;
- Arnaud, Pauline;
- Boileau, Catherine;
- Romefort, Bénédicte;
- Benbrik, Nadir;
- Gournay, Véronique;
- Joram, Nicolas;
- Baron, Olivier;
- Isidor, Bertrand
Publication type:
Article
Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.
Published in:
Molecular Syndromology, 2016, v. 6, n. 6, p. 287, doi. 10.1159/000443708
By:
- Sivasankaran, Aswini;
- Srikanth, Ambika;
- Kulshreshtha, Pooja S.;
- Anuradha, Deenadayalu;
- Kadandale, Jayarama S.;
- Samuel, Chandra R.
Publication type:
Article
Partial 1q Duplications and Associated Phenotype.
Published in:
Molecular Syndromology, 2016, v. 6, n. 6, p. 297, doi. 10.1159/000443599
By:
- Morris, Marcos L.M.;
- Baroneza, José E.;
- Teixeira, Patricia;
- Medina, Cristina T.N.;
- Cordoba, Mara S.;
- Versiani, Beatriz R.;
- Roese, Liege L.;
- Freitas, Erika L.;
- Fonseca, Ana C.S.;
- dos Santos, Maria C.G.;
- Pic-Taylor, Aline;
- Rosenberg, Carla;
- Oliveira, Silviene F.;
- Ferrari, Iris;
- Mazzeu, Juliana F.
Publication type:
Article
Differing Microdeletion Sizes and Breakpoints in Chromosome 7q11.23 in Williams-Beuren Syndrome Detected by Chromosomal Microarray Analysis.
Published in:
Molecular Syndromology, 2016, v. 6, n. 6, p. 268, doi. 10.1159/000443942
By:
- Li, Lin;
- Huang, Linhuan;
- Luo, Yanmin;
- Huang, Xuan;
- Lin, Shaobin;
- Fang, Qun
Publication type:
Article

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