Prenatal detection of trisomy 21 on nucleated red blood cells enriched from maternal circulation by using fluorescence in situ hybridization [4]

Prenatal Diagnosis

Volumn 22, Issue 9, 2002, Pages 836-839

  Hromadnikova, Ilona ^a   Hridelova, Dana ^a   Houbova, Bela ^a   Vavrinec, Jan ^a   Kofer, Josef ^b   Krofta, Ladislav ^c   Calda, Pavel ^d  

^a UNIVERSITY HOSPITAL MOTOL   (Czech Republic)

^b MASARYK UNIVERSITY   (Czech Republic)

^c INSTITUTE FOR THE CARE OF MOTHER AND CHILD   (Czech Republic)

^d CHARLES UNIVERSITY   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CLINICAL ARTICLE; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; ERYTHROCYTE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INTERMETHOD COMPARISON; KARYOTYPE; LETTER; MATERNAL AGE; MATERNAL BLOOD; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SCREENING TEST; TRISOMY 21;

ADULT; CELL NUCLEUS; DOWN SYNDROME; ERYTHROCYTE COUNT; ERYTHROCYTES; FEMALE; FETAL BLOOD; GESTATIONAL AGE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MATERNAL AGE; PREGNANCY; PREGNANCY, HIGH-RISK; PRENATAL DIAGNOSIS; SINGLE-BLIND METHOD;

EID: 0036733344     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.417     Document Type: Letter

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