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Placental transcriptomes in the common aneuploidies reveal critical regions on the trisomic chromosomes and genome-wide effects.
Bianco, Katherine; Gormley, Matthew; Farrell, Jason; Zhou, Yan; Oliverio, Oliver; Tilden, Hannah; McMaster, Michael; Fisher, Susan J.
Afiliação
  • Bianco K; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, CA, USA.
  • Gormley M; Center for Reproductive Sciences, Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, CA, USA.
  • Farrell J; The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA, USA.
  • Zhou Y; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Stanford University School of Medicine, Stanford, CA, USA.
  • Oliverio O; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, CA, USA.
  • Tilden H; Center for Reproductive Sciences, Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, CA, USA.
  • McMaster M; The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA, USA.
  • Fisher SJ; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, CA, USA.
Prenat Diagn ; 36(9): 812-22, 2016 Sep.
Article em En | MEDLINE | ID: mdl-27328057
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Down / Transtornos Cromossômicos Limite: Female / Humans / Pregnancy Idioma: En Revista: Prenat Diagn Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Down / Transtornos Cromossômicos Limite: Female / Humans / Pregnancy Idioma: En Revista: Prenat Diagn Ano de publicação: 2016 Tipo de documento: Article