A rare case of de novo distal 19q trisomy prenatally diagnosed

Prenatal Diagnosis

Volumn 24, Issue 10, 2004, Pages 822-827

  Rombout, Sonia ^a,b   Sartenaer, Daniel ^a   Parmentier, Benoît ^a   Dugauquier, Christian ^a   Gillerot, Yves ^a  

^a INSTITUTE OF PATHOLOGY AND GENETICS   (Belgium)

^b NONE   (Belgium)

Author keywords

Prenatal; Trisomy 19q

Indexed keywords

ADULT; ARTICLE; AUTOPSY; CASE REPORT; CHROMOSOME 19Q; CHROMOSOME ABERRATION; CYTOGENETICS; DE NOVO STUDY; DISEASE ASSOCIATION; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RARE DISEASE; TRISOMY;

ABNORMALITIES, MULTIPLE; ADULT; AMNIOCENTESIS; AMNIOTIC FLUID; CHROMOSOMES, HUMAN, PAIR 19; CHROMOSOMES, HUMAN, PAIR 22; CYTOGENETIC ANALYSIS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; PREGNANCY; PRENATAL DIAGNOSIS; TRANSLOCATION, GENETIC; TRISOMY;

EID: 7944229837     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.995     Document Type: Article

References (15)

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