Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues

Prenatal Diagnosis

Volumn 16, Issue 10, 1996, Pages 893-897

  Micale, M A ^a,c   Wolff, D J ^a   Dickerman, L H ^a   Redline, R ^b   Conroy, J M ^a   Schwartz, S ^a  

^a UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

^b CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c MEDICAL COLLEGE OF OHIO   (United States)

Author keywords

Fetal blood; FISH; Mosaicism; PCR; Trisomy 20

Indexed keywords

SATELLITE DNA;

AMNIOCENTESIS; AMNION CELL; ARTICLE; AUTOSOME MOSAICISM; CASE REPORT; CHORION VILLUS; FETUS; FETUS BLOOD; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; LYMPH NODE; METAPHASE; MOLECULAR GENETICS; POLYMERASE CHAIN REACTION; PREGNANCY TERMINATION; PRIORITY JOURNAL; SMALL INTESTINE; SUPERNUMERARY CHROMOSOME; TRISOMY;

ADULT; AMNIOCENTESIS; AMNIOTIC FLUID; CELLS, CULTURED; CHROMOSOMES, HUMAN, PAIR 20; FEMALE; FETAL BLOOD; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; MOSAICISM; POLYMERASE CHAIN REACTION; PREGNANCY; TRISOMY; ULTRASONOGRAPHY, PRENATAL;

EID: 0029848904     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199610)16:10<893::AID-PD962>3.0.CO;2-M     Document Type: Article

References (13)

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