Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotyping

Prenatal Diagnosis

Volumn 19, Issue 5, 1999, Pages 480-482

  Ning, Yi ^a,d   Laundon, Caroline H ^b   Schröck, Evelin ^c   Buchanan, Philip ^a,b   Ried, Thomas ^c  

^a GEORGE WASHINGTON UNIVERSITY   (United States)

^b GeneCare Medical Genetics Center   (United States)

^c NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^d Ross Hall   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNIOTIC FLUID CELL; ARTICLE; CASE REPORT; CENTROMERE; CHROMOSOME 14; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; CHROMOSOME MOSAICISM; CHROMOSOME NOR; DNA PROBE; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC COUNSELING; HUMAN; HUMAN CELL; KARYOTYPING; MALE; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RING CHROMOSOME; TELOMERE;

ADULT; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; FEMALE; FETAL DISEASES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MOSAICISM; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 0032950170     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199905)19:5<480::AID-PD547>3.0.CO;2-H     Document Type: Article

References (8)

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