Trisomy 12 mosaicism in CVS culture confirmed in the fetus [2]

Prenatal Diagnosis

Volumn 19, Issue 12, 1999, Pages 1176-1177

  Sikkema Raddatz, B ^a   Bouman, K ^a   Verschuuren Bemelmans, C C ^a   De Jong, B ^a  

^a UNIVERSITY OF GRONINGEN   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AMNIOCENTESIS; CASE REPORT; CHORION VILLUS SAMPLING; CHROMOSOME 12; CHROMOSOME MOSAICISM; FETUS; FETUS ECHOGRAPHY; GENETIC COUNSELING; HUMAN; LETTER; MATERNAL AGE; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TRISOMY; TRISOMY 12;

EID: 0032703213     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1097-0223(199912)19:12<1176::aid-pd710>3.0.co;2-%23     Document Type: Letter

References (3)

1. Hahnemann JM, Vejerslev LO. 1997. European Collaborative Research on Mosaicism in CVS (EUCROMIC) - Fetal and extrafetal cell lineages in 192 gestations with CVS mosaicism involving single autosomal trisomy. Am J Med Genet 70: 179-187.
2. Hsu LYF, Yu M-T, Neu RL, van Dyke DL, Benn PA, Bradshaw CL, Shaffer LG, Higgins RR, Khodr GS, Morton CC, Wang H, Brothman AR, Chadwick D, Disteche CM, Jenkins LS, Kalousek DK, Pantzar TJ, Wyatt P. 1997. Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations. Prenat Diagn 17: 201-242.
3. van Koskull H, Ritvanen A, Ämmälä P, Gahmberg N, Salonen R. 1989. Trisomy 12 mosaicism in amniocytes and dysmorphic child despite normal chromosomes in fetal blood sample. Prenat Diagn 9: 433-437.