Trisomy 7 mosaicism: Prognosis after prenatal diagnosis [2]

Prenatal Diagnosis

Volumn 22, Issue 13, 2002, Pages 1239-1240

  Warburton, Dorothy ^a  

^a Columbia University ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

URIDINE DIPHOSPHATE;

AMNIOCENTESIS; AMNION FLUID; CHROMOSOME ANALYSIS; HUMAN; LETTER; MITOSIS; MOSAICISM; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PROGNOSIS; RISK; TRISOMY 7;

ADULT; AMNIOCENTESIS; CHORIONIC VILLI SAMPLING; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 7; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; INFANT, NEWBORN; MOSAICISM; PREGNANCY; PRENATAL DIAGNOSIS; PROGNOSIS; TRISOMY; UNIPARENTAL DISOMY;

EID: 0036933177     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.482     Document Type: Letter

References (4)

1. Hahnemann JM, Vejersley 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 LY, Yu MT, Neu RL, et al. 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. Kalousek DK, Langlois S, Robinson WP, et al. 1996. Trisomy 7 CVS mosaicism: Pregnancy outcome, placental and DNA analysis in 14 cases. Am J Med Genet 65: 348-352.
4. Kivirikko S, Salonen R, Salo A, et al. 2002. Prenatally detected trisomy 7 mosaicism in a dysmorphic child. Prenat Diagn 22: 541-544.