-
1دورية أكاديمية
المؤلفون: Nasrin Malekpour, Rahim Vakili, Tayebeh Hamzehloie
المصدر: Iranian Journal of Basic Medical Sciences, Vol 21, Iss 9, Pp 950-956 (2018)
مصطلحات موضوعية: ARSB gene, Arylsulfatase B, Consanguineous marriage, DNA sequencing, Maroteaux-Lamy syndrome, Mucopolysaccharidosis VI (MPS VI), Medicine
وصف الملف: electronic resource
-
2دورية أكاديمية
المؤلفون: Mahdieh Davoodnejad, Peyman Eshraghi, Rahim vakili, Tayebeh Hamzehloie
المصدر: Egyptian Journal of Medical Human Genetics, Vol 18, Iss 2, Pp 165-172 (2017)
مصطلحات موضوعية: X-linked adrenal hypoplasia congenital (X-linked AHC), DAX1 protein, NR0B1 gene, Medicine (General), R5-920, Genetics, QH426-470
وصف الملف: electronic resource
-
3دورية أكاديمية
المصدر: Iranian Journal of Medical Sciences, Vol 37, Iss 1, Pp 3-8 (2012)
مصطلحات موضوعية: TP53, CHK1, CHK2, MDM2, Li-Fraumeni syndrome, tumor suppressor, Medicine (General), R5-920
وصف الملف: electronic resource
-
4
المؤلفون: Elmira Iranifar, Tayebeh Hamzehloie
المصدر: Open Journal of Genetics. :87-95
مصطلحات موضوعية: 0301 basic medicine, Apolipoprotein E, Genetics, Down syndrome, 030219 obstetrics & reproductive medicine, Biology, medicine.disease, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Nondisjunction, Polymorphism (computer science), medicine, Allele, Risk factor, Genotyping, Allele frequency
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::66f9bc1e86dcd3f4da483ba5236cddb5
https://doi.org/10.4236/ojgen.2016.64010 -
5
المؤلفون: Tayebeh Hamzehloie, Peyman Eshraghi, Rahim Vakili, Mahdieh Davoodnejad
المصدر: Egyptian Journal of Medical Human Genetics; Vol 18, No 2 (2017); 165-172
Egyptian Journal of Medical Human Genetics, Vol 18, Iss 2, Pp 165-172 (2017)مصطلحات موضوعية: 0301 basic medicine, lcsh:QH426-470, 030209 endocrinology & metabolism, Biology, medicine.disease_cause, 03 medical and health sciences, 0302 clinical medicine, Hypogonadotropic hypogonadism, Gene expression, medicine, Missense mutation, Genetics(clinical), Gene, Genetics (clinical), Genetics, lcsh:R5-920, Mutation, DAX1 protein, Adrenal hypoplasia, medicine.disease, Molecular biology, NR0B1 gene, lcsh:Genetics, 030104 developmental biology, Congenital adrenal hypoplasia, X-linked adrenal hypoplasia congenital (X-linked AHC), DAX1, lcsh:Medicine (General)
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52dc4aca14294af758311e19bb139a4a