A fetus with trisomy 9p and trisomy 10p originating from unbalanced segregation of a maternal complex chromosome rearrangement t(4;10;9)

Fetal Diagnosis and Therapy

Volumn 17, Issue 4, 2002, Pages 243-246

  Hengstschläger, Markus ^a   Bettelheim, Dieter ^a   Repa, Christa ^a   Lang, Susanna ^a   Deutinger, Josef ^a   Bernaschek, Gerhard ^a  

^a UNIVERSITY OF VIENNA   (Austria)

Author keywords

Complex chromosome rearrangement; FISH analysis; Prenatal diagnosis; Trisomy 10p; Trisomy 9p

Indexed keywords

ADULT; AMNION CELL; APLASIA; ARTICLE; AUTOPSY; BRAIN MALFORMATION; CASE REPORT; CHROMOSOME 10; CHROMOSOME 4; CHROMOSOME 9; CHROMOSOME REARRANGEMENT; CHROMOSOME SEGREGATION; CHROMOSOME TRANSLOCATION; CLEFT LIP PALATE; CLUBFOOT; CYTOGENETICS; FEMALE; FETUS; FETUS KARYOTYPING; FLUORESCENCE IN SITU HYBRIDIZATION; HETEROZYGOTE; HUMAN; KARYOTYPE 46,XX; KIDNEY POLYCYSTIC DISEASE; LOW SET EAR; LUNG MALFORMATION; NOSE MALFORMATION; PARTIAL TRISOMY 10; PARTIAL TRISOMY 9; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; ULTRASOUND; UTERUS DISEASE; GENE TRANSLOCATION; GENETICS; MULTIPLE MALFORMATION SYNDROME; PREGNANCY; TRISOMY;

ABNORMALITIES, MULTIPLE; ADULT; CASE REPORT; CHROMOSOME SEGREGATION; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 4; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; HUMAN; IN SITU HYBRIDIZATION, FLUORESCENCE; PREGNANCY; PRENATAL DIAGNOSIS; TRANSLOCATION (GENETICS); TRISOMY; HUMANS; TRANSLOCATION, GENETIC;

EID: 0035989302     PISSN: 10153837     EISSN: None     Source Type: Journal    
DOI: 10.1159/000063401     Document Type: Article

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11. Molecular cytogenetics, RFLP analysis and clinical characterization of a de novo trisomy 10p case