Normal prenatal ultrasound findings in a case with de novo mosaic small supernumerary marker chromosome 18 how to counsel?

Journal of Maternal-Fetal and Neonatal Medicine

Volumn 25, Issue 2, 2012, Pages 200-202

  Eckmann Scholz, Christel ^a   Tönnies, Holger ^a   Liehr, Thomas ^b   Gesk, Stefan ^a   Jonat, Walter ^a   Caliebe, Almuth ^b  

^a UNIVERSITY OF KIEL   (Germany)

^b JENA UNIVERSITY HOSPITAL   (Germany)

Author keywords

Mosaic trisomy 18; Prenatal ultrasound; Small supernumerary marker chromosomes

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME 18; CHROMOSOME ANALYSIS; CHROMOSOME BANDING PATTERN; CHROMOSOME MARKER; CHROMOSOME MOSAICISM; COMPARATIVE GENOMIC HYBRIDIZATION; EUCHROMATIN; FEMALE; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; GENETIC COUNSELING; GENETIC SCREENING; HUMAN; KARYOTYPING; NEWBORN; PARENT COUNSELING; PHENOTYPE; POSTNATAL CARE; PREGNANCY OUTCOME; PRENATAL SCREENING; PRIORITY JOURNAL; SUPERNUMERARY CHROMOSOME; TRISOMY 18;

ADULT; AMNIOCENTESIS; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; GENETIC COUNSELING; HUMANS; MOSAICISM; PREGNANCY; ULTRASONOGRAPHY, PRENATAL;

EID: 84855658651     PISSN: 14767058     EISSN: 14764954     Source Type: Journal    
DOI: 10.3109/14767058.2011.566949     Document Type: Article

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