Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency : Molecular cytogenetic analysis and review of the literature
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概要
- 論文の詳細を見る
- 2010-04-01
著者
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Liehr Thomas
Institute Of Human Genetics Jena University
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Petersen Michael
Department Of Genetics Institute Of Child Health 'aghia Sophia' Children's Hospital
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PETERSEN Michael
Department of Genetics, Institute of Child Health, Aghia.Sophia Children's Hospital
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MANOLAKOS Emmanouil
Vioiatriki SA Molecular Diagnostics Laboratory, Institute of Child Health, Aghia Sophia Children's Hospital
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PEITSIDIS Panagiotis
Department of Fetal Medicine, Royal Free Hospital
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ELEFTHERIADES Makarios
EmbryoCare, Fetal Medicine Centre, Institute of Child Health, Aghia.Sophia Children's Hospital
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DEDOULIS Evaggelos
GYNH Research Center for Prenatal Diagnosis, Institute of Child Health, Aghia.Sophia Children's Hospital
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ZIEGLER Monika
Institute of Human Genetics and Anthropology
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ORRU Sandro
Department of Medical Genetics, University of Cagliari
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MANOLAKOS Emmanouil
Vioiatriki SA Molecular Diagnostics Laboratory, Institute of Child Health, Aghia Sophia Children's Hospital
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ELEFTHERIADES Makarios
EmbryoCare, Fetal Medicine Centre, Institute of Child Health, Aghia.Sophia Children's Hospital
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LIEHR Thomas
Institute of Human Genetics and Anthropology
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DEDOULIS Evaggelos
GYNH Research Center for Prenatal Diagnosis, Institute of Child Health, Aghia.Sophia Children's Hospital
関連論文
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- Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency : Molecular cytogenetic analysis and review of the literature