Roberts syndrome: Clinical and cytogenetic studies in 8 Egyptian patients and molecular studies in 4 patients with genotype/phenotype correlation

Autor:	Ismail, S., Essawi, M., Sedky, N., Hassan, H., Fayez, A., Helmy, N., Shehab, M., Farouk, D., Elruby, M., Otaify, G., Eldarsh, A., Hosny, L., Gaber, K., Aboul-Ezz, E. H. A., Ramzy, M. I., MennatAllah I. Mehrez, Hassib, N. F., Elhadidi, S. M. A., Aglan, M. S., Temtamy, S. A.
Zdroj:	Scopus-Elsevier
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::08352f383ea6b5069224a75a731a5d1f http://www.scopus.com/inward/record.url?eid=2-s2.0-85015211027&partnerID=MN8TOARS Zobrazit plný text záznamu