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1دورية أكاديمية
المؤلفون: Ahmed A. Baz, Elsayed K. Bakhiet, Usama Abdul-Raouf, Ahmed Abdelkhalek
المصدر: Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-12 (2021)
مصطلحات موضوعية: Staphylococcus aureus, Antibiotic resistance, Enterotoxin, Real-time PCR, Medicine (General), R5-920, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2090-2441Test
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2دورية أكاديمية
المصدر: Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-7 (2021)
مصطلحات موضوعية: Vitamin D, Nocturnal enuresis, Children, Primary mono-symptomatic, Medicine (General), R5-920, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2090-2441Test
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3دورية أكاديمية
المصدر: Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-5 (2020)
مصطلحات موضوعية: Perforin (PRF1), Familial hemophagocytic lymphohistiocytosis 2 (FHL 2), Case report, Novel mutation, Medicine (General), R5-920, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: http://link.springer.com/article/10.1186/s43042-020-00067-3Test; https://doaj.org/toc/2090-2441Test
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4دورية أكاديمية
المؤلفون: Farida El-Baz, Mohamed E. Mowafy, Ahmed Lotfy
المصدر: Egyptian Journal of Medical Human Genetics, Vol 19, Iss 2, Pp 113-116 (2018)
مصطلحات موضوعية: Medicine (General), R5-920, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: http://www.sciencedirect.com/science/article/pii/S1110863017300745Test; https://doaj.org/toc/1110-8630Test
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5دورية أكاديمية
المؤلفون: Farida El-Baz Mohamed, Rasha T. Hamza, Nermine H. Amr, Azza M. Youssef, Tarek M. Kamal, Rana A. Mahmoud
المصدر: Egyptian Journal of Medical Human Genetics, Vol 18, Iss 1, Pp 67-73 (2017)
مصطلحات موضوعية: Childhood obesity, POMC gene, Metabolic syndrome, Medicine (General), R5-920, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: http://www.sciencedirect.com/science/article/pii/S111086301600029XTest; https://doaj.org/toc/1110-8630Test
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6دورية أكاديمية
المؤلفون: Farida El-Baz, Mohamed Saad Zaghloul, Ezzat El Sobky, Reham M Elhossiny, Heba Salah, Neveen Ezy Abdelaziz
المصدر: Egyptian Journal of Medical Human Genetics, Vol 17, Iss 1, Pp 57-62 (2016)
مصطلحات موضوعية: Autism, Chromosomal abnormality, High resolution karyotype, Medicine (General), R5-920, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: http://www.sciencedirect.com/science/article/pii/S111086301500049XTest; https://doaj.org/toc/1110-8630Test
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7دورية أكاديمية
المؤلفون: Rabah M. Shawky, Farida El-baz, Tarek M. Kamal, Reham M. Elhossiny, Mona A. Ahmed, Ghada H. El Nady
المصدر: Egyptian Journal of Medical Human Genetics, Vol 15, Iss 4, Pp 335-341 (2014)
مصطلحات موضوعية: Autism, MTHFR gene, Polymorphism, Genotype–phenotype, Egyptian children, Medicine (General), R5-920, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: http://www.sciencedirect.com/science/article/pii/S1110863014000603Test; https://doaj.org/toc/1110-8630Test
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8دورية أكاديمية
المؤلفون: Farida El-baz, Reham M. Elhossiny, Yasser Abdel Azeem, Marianne Girgis
المصدر: Egyptian Journal of Medical Human Genetics, Vol 15, Iss 2, Pp 155-162 (2014)
مصطلحات موضوعية: Autism, Hyperbaric oxygen therapy, Oxidative stress, Behavior, Medicine (General), R5-920, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: http://www.sciencedirect.com/science/article/pii/S1110863014000214Test; https://doaj.org/toc/1110-8630Test
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9
المصدر: Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-5 (2020)
مصطلحات موضوعية: 0301 basic medicine, Novel mutation, lcsh:QH426-470, Hepatosplenomegaly, Frameshift mutation, Perforin (PRF1), 03 medical and health sciences, Exon, 0302 clinical medicine, Case report, medicine, Cytotoxic T cell, Familial hemophagocytic lymphohistiocytosis 2 (FHL 2), Genetics (clinical), lcsh:R5-920, Hemophagocytic lymphohistiocytosis, biology, Familial Hemophagocytic Lymphohistiocytosis, medicine.disease, lcsh:Genetics, 030104 developmental biology, Perforin, Granzyme, 030220 oncology & carcinogenesis, Immunology, biology.protein, medicine.symptom, lcsh:Medicine (General)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f9a652abbffb131724183c45305decdTest
https://doi.org/10.1186/s43042-020-00067-3Test -
10
المؤلفون: Ahmed Lotfy, Farida El-Baz, Mohamed El-Sayed Mowafy
المصدر: Egyptian Journal of Medical Human Genetics, Vol 19, Iss 2, Pp 113-116 (2018)
Egyptian Journal of Medical Human Genetics; Vol 19, No 2 (2018); 113-116مصطلحات موضوعية: 0301 basic medicine, lcsh:QH426-470, Eye contact, Physiology, Physical examination, Autism, Copper, Ceruloplasmin, Stereotypic movements, 03 medical and health sciences, 0302 clinical medicine, Neurodevelopmental disorder, medicine, Medical history, Genetics (clinical), Motor skill, lcsh:R5-920, medicine.diagnostic_test, biology, business.industry, medicine.disease, lcsh:Genetics, 030104 developmental biology, biology.protein, Etiology, Autism, lcsh:Medicine (General), Ceruloplasmin, business, 030217 neurology & neurosurgery
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc77077662a80a0e15126541020869f8Test
https://doi.org/10.1016/j.ejmhg.2017.08.002Test