Trisomy 17 mosaicism in amniotic fluid cells not found at birth in blood but present in skin fibroblasts

Prenatal Diagnosis

Volumn 19, Issue 3, 1999, Pages 263-265

  Lesca, Gaetan ^a,b   Boggio, Dominique ^b   Bellec, Veronique ^c   Magaud, Jean Pierre ^a   Till, Marianne ^a  

^a EDOUARD HERRIOT HOSPITAL   (France)

^b HÔTEL DIEU   (France)

^c LMM Laboratoire Marcel Merieux   (France)

Author keywords

Amniotic fluid cells; Chromosome mosaicism; Cultured fibroblasts; Phenotype karyotype correlation; Trisomy 17

Indexed keywords

AMNIOCENTESIS; AMNIOTIC FLUID CELL; ARTICLE; CASE REPORT; CHROMOSOME 17; CHROMOSOME MOSAICISM; CLINICAL EXAMINATION; DNA PROBE; FEMALE; FETUS; HUMAN; HUMAN CELL; IN SITU HYBRIDIZATION; KARYOTYPE; LYMPHOCYTE; PRIORITY JOURNAL; SKIN FIBROBLAST; TRISOMY; UMBILICAL CORD BLOOD;

AMNIOTIC FLUID; CELLS, CULTURED; CHROMOSOMES, HUMAN, PAIR 17; FIBROBLASTS; HUMANS; INFANT, NEWBORN; KARYOTYPING; LYMPHOCYTES; MALE; MATERNAL AGE; MOSAICISM; PHENOTYPE; SKIN; TRISOMY; TWINS;

EID: 0033048176     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199903)19:3<263::AID-PD506>3.0.CO;2-0     Document Type: Article

References (10)

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