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1 Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies [期刊论文]

来源：Molecular Cytogenetics

作者:Yuri B Yurov;Alexandra P Silvanovich;Maria A Zelenova;等

关键词:Copy number viriations (CNVs);Chromosome abnormalities;...

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2 Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome? [期刊论文]

来源：Molecular Cytogenetics

作者:Yao-Shan Fan;Maria Buch;Mustafa Tekin;等

关键词:Copy number variations (CNVs);Array CGH;...

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3 Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome? [期刊论文]

来源：Molecular Cytogenetics

作者:Yao-Shan Fan;Maria Buch;Mustafa Tekin;等

关键词:Copy number variations (CNVs);Array CGH;...

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4 Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies [期刊论文]

来源：Molecular Cytogenetics

作者:Yuri B Yurov;Alexandra P Silvanovich;Maria A Zelenova;等

关键词:Copy number viriations (CNVs);Chromosome abnormalities;...

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5 Identification of small segmental translocations in patients with repeated implantation failure and recurrent miscarriage using next generation sequencing after in vitro fertilization/intracytoplasmic sperm injection [期刊论文]

来源：Molecular Cytogenetics

作者:Hong Li;Chunhua Lin;Qiang Liu;等

关键词:Translocation;RM;...

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6 Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype [期刊论文]

来源：Molecular Cytogenetics

作者:Bela Melegh;Katalin Komlosi;Balazs Duga;等

关键词:Supernumerary chromosome;15q duplication syndrome;...

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