Fetoplacental and fetoamniotic chromosomal discrepancies in prenatally detected mosaic trisomy 9 [2]

Prenatal Diagnosis

Volumn 23, Issue 12, 2003, Pages 1019-1021

  Chen, Chih Ping ^a,b   Chern, Schu Rern ^a   Town, Dai Dyi ^a   Wang, Wayseen ^a   Liao, You Wei ^c  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

^b NATIONAL YANG MING UNIVERSITY   (Taiwan)

^c TAIWAN ADVENTIST HOSPITAL   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNIOCENTESIS; AMNION CELL; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME DISORDER; CHROMOSOME MOSAICISM; CLINICAL FEATURE; FEMALE; FETUS; FETUS MALFORMATION; HUMAN; LETTER; PRIORITY JOURNAL; TRISOMY; TRISOMY 9;

ABORTION, INDUCED; ADULT; AMNIOCENTESIS; AMNION; CHROMOSOMES, HUMAN, PAIR 9; DIAGNOSIS, DIFFERENTIAL; FEMALE; GENETIC SCREENING; HUMANS; MALE; MATERNAL AGE; PEDIGREE; PLACENTA; PREGNANCY; PREGNANCY TRIMESTER, SECOND; PREGNANCY, HIGH-RISK; PRENATAL DIAGNOSIS; TRISOMY;

EID: 0347478049     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.725     Document Type: Letter

References (2)

1. Arnold GL, Kirby RS, Stern TP, Sawyer JR. 1995. Trisomy 9: review and report of two new cases. Am J Med Genet 56: 252-257.
2. Hsu LYF, Yu M-T, Neu R-L, 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.