Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16

Prenatal Diagnosis

Volumn 21, Issue 6, 2001, Pages 477-480

  Hengstschläger, Markus ^a   Bettelheim, Dieter ^a   Drahonsky, Regina ^a   Deutinger, Josef ^a   Bernaschek, Gerhard ^a  

^a UNIVERSITY OF VIENNA   (Austria)

Author keywords

Chromosome 16; FISH analysis; Mosaicism; Prenatal diagnosis; Supernumerary marker

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 16; CHROMOSOME IDENTIFICATION; CHROMOSOME MARKER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MOSAICISM; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RISK ASSESSMENT; SUPERNUMERARY CHROMOSOME;

ABORTION, INDUCED; ADULT; ANEUPLOIDY; CHROMOSOMES, HUMAN, PAIR 16; DIAGNOSIS, DIFFERENTIAL; FEMALE; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 0034924805     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.95     Document Type: Article

References (20)

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15. Prenatal supernumerary r(16) chromosome characterized by multiprobe FISH with normal pregnancy outcome
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17. Familial supernumerary nonsatellited microchromosome
18. De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: Clinical significance and distribution of breakpoints