Zobrazeno 1 - 3
of 3
pro vyhledávání: '"M. Y. Issa"'
Autor:
A. M. Mohamed, H. T. El-Bassyouni, A. M. El-Gerzawy, S. A. Hammad, N. A. Helmy, A. K. Kamel, S. I. Ismail, M. Y. Issa, O. Eid, M. S. Zaki
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-10 (2018)
Abstract Background Microdeletion of 1q43q44 causes a syndrome characterized by intellectual disability (ID), speech delay, seizures, microcephaly (MIC), corpus callosum abnormalities (CCA) and characteristic facial features. Duplication of 4q is pre
Externí odkaz:
https://doaj.org/article/4bb3e3b49d954110af41fd84ef51a065
Autor:
S R, Emam, R M, Abd-Elsalam, A A, Azouz, S E, Ali, S A, El Badawy, M A, Ibrahim, B B, Hassan, M Y, Issa, S H, Elmosalamy
Publikováno v:
Journal of physiology and pharmacology : an official journal of the Polish Physiological Society. 72(1)
The safety and effectiveness of nutricetics suggest that they may offer an alternative to pharmaceutical and surgical therapy for hormone-dependent disorders, such as polycystic ovarian syndrome (PCOS). We investigated the effects of Linum usitatissi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::379c7d010ecbc5fece1eb295cdbdb523
https://pubmed.ncbi.nlm.nih.gov/34099585
https://pubmed.ncbi.nlm.nih.gov/34099585
Publikováno v:
Clinical genetics. 93(1)
Hyperphosphatasia with mental retardation syndrome (HPMRS) is caused by recessive mutations in genes involved in the glycosylphosphatidylinsitol pathway, including PGAP3.We describe 10 patients from 8 Egyptian families presenting with developmental d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0afd29bbd9616cf9cafe22a5060b9455
https://pubmed.ncbi.nlm.nih.gov/28390064
https://pubmed.ncbi.nlm.nih.gov/28390064