Prenatally detected trisomy 20 mosaicism and genetic counseling [6]

Prenatal Diagnosis

Volumn 25, Issue 8, 2005, Pages 725-726

  Bianca, S ^a   Ingegnosi, C ^a   Tetto, C ^b   Cataliotti, A ^a   Ettore, G ^b  

^a Centro di Consulenza Genetica e di Teratologia della Riproduzione   (Italy)

^b UO Ginecologia e Ostetricia   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMNIOCENTESIS; BLOOD SAMPLING; CHORION VILLUS; CHROMOSOME MOSAICISM; DOWN SYNDROME; ECHOGRAPHY; FETUS BLOOD; GENETIC ANALYSIS; GENETIC COUNSELING; HUMAN; INTRAUTERINE GROWTH RETARDATION; LETTER; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SPONTANEOUS ABORTION; TRISOMY; TRISOMY 20;

CHROMOSOMES, HUMAN, PAIR 20; GENETIC COUNSELING; HUMANS; KARYOTYPING; MOSAICISM; PRENATAL DIAGNOSIS; RISK FACTORS; TRISOMY;

EID: 23844457617     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1232     Document Type: Letter

References (3)

1. Gardner RJM, Sutherland GR. 1996. Chromosome Abnormalities and Genetic Counseling. Oxford University Press: New York.
2. Hsu LYF, Kaffe S, Perlis TE. 1987. Trisomy 20 mosaicism in prenatal diagnosis-a review and update. Prenat Diagn 7: 581-596.
3. Robinson WP, McGillivray B, Lewis MES, et al. 2005. Prenatally detected trisomy 20 mosaicism. Prenat Diagn 25: 239-244.