Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Helmy, Nivine A."'
Autor:
Meguid, Nagwa A., Eid, Maha M., Mohamed, Amal M., Ghanoum, Heba, Helmy, Nivine A., Eid, Ola M.
Publikováno v:
In Research in Autism Spectrum Disorders June 2018 50:43-50
Autor:
Refaat, Khaled, Helmy, Nivine, Elawady, Mohamed, El Ruby, Mona, Kamel, Alaa, Mekkawy, Mona, Ashaat, Engy, Eid, Ola, Mohamed, Amal, Rady, Mervat
Publikováno v:
Mol Syndromol
Mowat-Wilson syndrome (MWS) is a rare autosomal dominant syndrome characterized by dysmorphic features, mental retardation, and congenital heart disease (CHD). MWS results from microdeletions of chromosome 2q23 or de novo SNVs involving the ZEB2 gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c5ced1088163188616a5018ea595f732
https://europepmc.org/articles/PMC8114072/
https://europepmc.org/articles/PMC8114072/
Akademický článek
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Autor:
Fadel, Islam M., Ragab, Moustafa H., Eid, Ola M., Helmy, Nivine A., El-Bassyouni, Hala T., Mazen, Inas
Publikováno v:
Journal of Genetic Engineering & Biotechnology; 7/28/2021, Vol. 19 Issue 1, p1-7, 7p
Autor:
Mekkawy, Mona K., Kamel, Alaa K., Thomas, Manal M., Ashaat, Engy A., Zaki, Maha S., Eid, Ola M., Ismail, Samira, Hammad, Saida A., Megahed, Hisham, ElAwady, Heba, Refaat, Khaled M., Hussien, Shymaa, Helmy, Nivine, Abd Allah, Sally G., Mohamed, Amal M., El Ruby, Mona O.
Publikováno v:
Molecular Genetics & Genomic Medicine; Feb2021, Vol. 9 Issue 2, p1-17, 17p
Autor:
Refaat, Khaled, Helmy, Nivine, Elawady, Mohamed, El Ruby, Mona, Kamel, Alaa, Mekkawy, Mona, Ashaat, Engy, Eid, Ola, Mohamed, Amal, Rady, Mervat
Publikováno v:
Molecular Syndromology; 20210101, Issue: Preprints p1-9, 9p
Autor:
Hussen, Dalia, Kamel, Alaa, Mekkawy, Mona, Mohamed, Amal, Zaki, Maha, Issa, Mahmoud, El Ruby, Mona, Ashaat, Engy, Ismail, Samira, Refaat, Khaled, Helmy, Nivine
Publikováno v:
Middle East Journal of Medical Genetics; Jul-Dec2019, Vol. 8 Issue 2, p158-168, 11p
Autor:
Issa, Mahmoud, Ismail, Samira, Helmy, Nivine, Kamel, Alaa, Amin, Sherine, Abdel Baky, Olweya, Zaki, Maha
Publikováno v:
Middle East Journal of Medical Genetics; Jul-Dec2018, Vol. 7 Issue 2, p88-95, 8p
Autor:
Ismail, Samira, Kamel, Alaa K., Eid, Maha M., Elruby, Mona O., Aglan, Mona S., Mekkawy, Mona K., Zaki, Maha S., Mohamed, Amal M., Helmy, Nivine A., Temtamy, Samia A.
Publikováno v:
Middle East Journal of Medical Genetics; Jan2017, Vol. 8 Issue 1, p29-34, 6p, 4 Color Photographs, 1 Chart
Autor:
Mohamed, Amal M., Kamel, Alaa K., Helmy, Nivine A., Hammad, Saida, Kayed, Hesham F., Shihab, Marwa, El-Gerzawy, Assad, Eid, Maha M., Eid, Ola M., Mekkawy, Mona K., Mahmoud, Wael, Mazen, Inas, El-Ruby, Mona, Afifi, Hanan, Zaki, Maha, Salam, Ghada A., Aglan, Mona, Temtamy, Samia
Publikováno v:
Middle East Journal of Medical Genetics; Jan2017, Vol. 8 Issue 1, p13-21, 9p, 7 Charts, 3 Graphs