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Volumn 28, Issue 8, 2008, Pages 764-766

Prenatal diagnosis of monosomy 18p involving a jumping translocation

Author keywords

Fetal and placental pathology; Fetal imaging; Fetal ultrasound; General cytogenetics; Jumping translocation; Monosomy 18p syndrome; Prenatal cytogenetics; QF PCR

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; BLOOD SAMPLING; CASE REPORT; CELL LINE; CHORION VILLUS SAMPLING; CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME ABERRATION; CHROMOSOME TRANSLOCATION; CYTOGENETICS; DOWN SYNDROME; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; HUMAN; HUMAN CELL; HUMAN TISSUE; INGUINAL HERNIA; JUMPING TRANSLOCATION; KARYOTYPE; KARYOTYPING; MONOSOMY; MONOSOMY 18P; MOSAICISM; ORCHIDOPEXY; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

EID: 49949118702     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.2030     Document Type: Article
Times cited : (7)

References (10)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.