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Volumn 28, Issue 8, 2008, Pages 764-766
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Prenatal diagnosis of monosomy 18p involving a jumping translocation
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Author keywords
Fetal and placental pathology; Fetal imaging; Fetal ultrasound; General cytogenetics; Jumping translocation; Monosomy 18p syndrome; Prenatal cytogenetics; QF PCR
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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;
ADULT;
CHORIONIC VILLI SAMPLING;
CHROMOSOMES, HUMAN, PAIR 18;
FEMALE;
HUMANS;
INFANT;
INFANT, NEWBORN;
MONOSOMY;
PREGNANCY;
PREGNANCY TRIMESTER, FIRST;
TRANSLOCATION, GENETIC;
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EID: 49949118702
PISSN: 01973851
EISSN: 10970223
Source Type: Journal
DOI: 10.1002/pd.2030 Document Type: Article |
Times cited : (7)
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References (10)
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