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Prenatal Diagnosis

Volumn 13, Issue 9, 1993, Pages 825-832

Application of fluorescent in situ hybridization for ‘de novo’ anomalies in prenatal diagnosis

(4) Van Opstal, D a Eussen, H J a Van Hemel, J O a Sachs, E S a

a ERASMUS UNIVERSITY ROTTERDAM (Netherlands)

Author keywords

In situ hybridization; Markers; Prenatal diagnosis

Indexed keywords

ARTICLE; AUTOPSY; CASE REPORT; CHROMOSOME ABERRATION; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; MALE; MARKER CHROMOSOME; PARTIAL TRISOMY; PRENATAL DIAGNOSIS;

ADULT; AMNIOCENTESIS; CASE REPORT; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 18; DANDY-WALKER SYNDROME; DNA PROBES; FEMALE; FETAL DISEASES; HUMAN; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; PREGNANCY; PREGNANCY TRIMESTER, SECOND; PREGNANCY TRIMESTER, THIRD; PRENATAL DIAGNOSIS; TRANSLOCATION (GENETICS); TRISOMY;

EID: 0027440149 PISSN: 01973851 EISSN: 10970223 Source Type: Journal
DOI: 10.1002/pd.1970130906 Document Type: Article

Times cited : (16)

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