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Autor:
M Yirmibes, Karaoguz, F, Bal, T, Yakut, N Ozturk, Ercelen, M A, Ergun, A Balci, Gokcen, A Asyali, Biri, Y, Kimya, B, Urman, M, Gultomruk, U, Egeli, S, Menevse
Publikováno v:
Genetic counseling (Geneva, Switzerland). 17(2)
The experience on prenatal chromosome diagnosis of four Turkish centers participating in a collaborative study on 6041 genetic amniocentesis performed during a 4-8 years period were reviewed. 5887 (97.5%) patients had strong clinical indications for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c8c4918400438e228ab1dc9372e94a01
https://pubmed.ncbi.nlm.nih.gov/16970041
https://pubmed.ncbi.nlm.nih.gov/16970041
