Trisomy 18 in neonates: prenatal diagnosis, clinical features, therapeutic dilemmas and outcome-Reference-Cited by-同舟云学术

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Trisomy 18 in neonates: prenatal diagnosis, clinical features, therapeutic dilemmas and outcome

Published:2006-06 Issue:2 Volume:47 Page:165-170
ISSN:1234-1983
Container-title:Journal of Applied Genetics
language:en
Short-container-title:J Appl Genet

Author:

Goc Barbara,Walencka Zofia,Włoch Agata,Wojciechowska Ewa,Więcek-Włodarska Danuta,Krzystolik-Ładzińska Joanna,Bober Klaudiusz,Świetliński Janusz

Publisher

Springer Science and Business Media LLC

Subject

Genetics,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF03194617.pdf

Reference17 articles.

1. Baty BJ, Blackburn BL, Carey JC, 1994. Natural history of trisomy 18 and trisomy 13: Growth, physical assessment, medical histories, survival, and recurrence risk. Am J Med Genet 49: 175–188.

2. Bos AP, Broers CJ, Hazebroek FW, van Hemel JO, Tibboel D, Wesby-Van Swaay E, Molenmar JC, 1992. Avoidance of emergency surgery in newborn infants with trisomy 18. Lancet 339: 913–917.

3. Carter PE, Pearn JH, Bell J, Martin N, Andreson NG, 1985. Survival in trisomy 18: life tables for use in genetic counselling and clinical paediatrics. Clin Genet 27: 59–61.

4. Chitty LS, 1995. Ultrasound screening for fetal abnormalities. Prenat Diagn 15: 1241–1257.

5. De Vigan C, Baena N, Cariati E, Clementi M, Stoll C, and the EUROSCAN working group, 2001. Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe. Ann Genet 44: 209–217.

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