Use of routinely collected amniotic fluid for whole-genome expression analysis of polygenic disorders.

Nagy, Gyula Richárd; Gyõrffy, Balázs; Galamb, Orsolya; Molnár, Béla; Nagy, Bálint; Papp, Zoltán

Nagy, Gyula Richárd; Gyõrffy, Balázs; Galamb, Orsolya; Molnár, Béla; Nagy, Bálint; Papp, Zoltán.

Affiliation

Nagy GR; 1st Department of Obstetrics and Gynecology, Semmelweis University, Budapest, Hungary. nagygyr@noi1.sote.hu

Clin Chem ; 52(11): 2013-20, 2006 Nov.

Article in En | MEDLINE | ID: mdl-17008366

Subject(s)

Amniotic Fluid; Genome/genetics; Multifactorial Inheritance/genetics; Neural Tube Defects/diagnosis; Neural Tube Defects/genetics; Oligonucleotide Array Sequence Analysis; Female; Humans; Neural Tube Defects/physiopathology; Pilot Projects; Pregnancy; RNA, Messenger/analysis

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Database: MEDLINE Main subject: Genome / Oligonucleotide Array Sequence Analysis / Multifactorial Inheritance / Amniotic Fluid / Neural Tube Defects Language: En Journal: Clin Chem Year: 2006 Type: Article Affiliation country: Hungary

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