Prediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseases-Reference-Cited by-同舟云学术

Prediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseases

Published:2011-05-06 Issue:2 Volume:2 Page:181-195
ISSN:1878-5077
Container-title:EPMA Journal
language:en
Short-container-title:EPMA Journal

Author:

Dundar Munis,Uzak Asli Subasioglu,Erdogan Murat,Akbarova Yagut

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry (medical),Health Policy,Drug Discovery

Link

https://link.springer.com/content/pdf/10.1007/s13167-011-0080-3.pdf

Reference102 articles.

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4. Stembalska A, Ryszard OE, Karolina P, Justyna G, Sasiadek MM. Prenatal diagnosis—principles of diagnostic procedures and genetic counseling. Folia Histochem Cytobiol. 2007;45(Supp. 1):11–6.

5. Han SH, An JW, Jeong GY, Yoon HR, Lee A, Yang YH, et al. Clinical and cytogenetic findings on 31,615 mid-trimester amniocenteses. Korean J Lab Med. 2008;28:378–85.

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