Early and rapid prenatal diagnosis of monosomy 2q36.1 in trophoblast cells

Fetal Diagnosis and Therapy

Volumn 21, Issue 5, 2006, Pages 428-432

  Tachdjian, Gérard ^a   Aboura, Azzedine ^a   Brisset, Sophie ^a   Dommergues, Marc ^a   Gajdos, Vincent ^a   Labrune, Philippe ^a  

^a HÔPITAL ANTOINE BÉCLÈRE   (France)

Author keywords

Chromosome 2; Fluorescence in situ hybridization; Monosomy; Prenatal diagnosis; Trophoblast cells

Indexed keywords

ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; CASE REPORT; CELL NUCLEUS; CHORION VILLUS; CHROMOSOME 2Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME INVERSION; CHROMOSOME REARRANGEMENT; EARLY DIAGNOSIS; FEMALE; FETUS; FETUS KARYOTYPING; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INTERPHASE; KARYOTYPE 46,XY; METAPHASE; MONOSOMY; MONOSOMY 2Q36.1; PARTIAL MONOSOMY; PRENATAL DIAGNOSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; TROPHOBLAST;

CHILD, PRESCHOOL; CHORIONIC VILLI SAMPLING; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 2; FEMALE; GENE DELETION; GESTATIONAL AGE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INVERSION, CHROMOSOME; MONOSOMY; PREGNANCY; PRENATAL DIAGNOSIS; TROPHOBLASTS;

EID: 33747321447     PISSN: 10153837     EISSN: None     Source Type: Journal    
DOI: 10.1159/000093885     Document Type: Article

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