Prenatal diagnosis of common aneuploidies using multiplex quantitative fluorescent polymerase chain reaction

Fetal Diagnosis and Therapy

Volumn 19, Issue 6, 2004, Pages 496-503

  El Mouatassim, S ^a   Becker, M ^a   Kuzio, S ^b   Ronsin, C ^c   Gil, S ^d   Nouchy, M ^a   Druard, L ^c   Forestier, F ^a  

^a LMM Laboratoire Marcel Merieux   (France)

^b INSTITUT DE RECHERCHES INTERNATIONALES SERVIER   (France)

^c Laboratoire d'Analyses Medicales du Dr Claude Levy   (France)

^d UNIVERSITÉ PARIS SACLAY   (France)

Author keywords

Down syndrome; Edward's syndrome; Patau's syndrome; Prenatal diagnosis; Quantitative fluorescent polymerase chain reaction; Trisomy

Indexed keywords

AMNION FLUID; ANEUPLOIDY; ARTICLE; CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME ANALYSIS; CONTROLLED STUDY; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RETROSPECTIVE STUDY; TANDEM REPEAT; TRISOMY 13; TRISOMY 18; TRISOMY 21;

ANEUPLOIDY; DOWN SYNDROME; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 8344258135     PISSN: 10153837     EISSN: None     Source Type: Journal    
DOI: 10.1159/000080162     Document Type: Article

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