المؤلفون: Mufti AH, AlJahdali IA, Elhawary NA, Ekram SN, Abumansour I, Sindi IA, Naffadi H, Elhawary EN, Alyamani NM, Alghamdi G, Alosaimi W, Rawas G, Alharbi A, Tayeb MT

المصدر: International Journal of General Medicine, Vol Volume 14, Pp 10031-10044 (2021)

مصطلحات موضوعية: vitiligo, tap1/psmb9, single nucleotide polymorphisms, taqman genotyping, linkage disequilibrium, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://www.dovepress.com/variations-in-tap1-and-psmb9-genes-involved-in-antigen-processing-and--peer-reviewed-fulltext-article-IJGM; https://doaj.org/toc/1178-7074

URL الوصول: https://doaj.org/article/0d7d1d0f2f484b0d8336293bf30392a3

المؤلفون: Sindi IA, Babalghith AO, Tayeb MT, Mufti AH, Naffadi H, Ekram SN, Elhawary EN, Alenezi M, Elhawary NA

المصدر: International Journal of General Medicine, Vol Volume 14, Pp 1311-1323 (2021)

مصطلحات موضوعية: colorectal carcinoma, single nucleotide polymorphism, taqman genotyping, linkage disequilibrium, age at diagnosis, nonsmokers, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://www.dovepress.com/risk-of-colorectal-carcinoma-may-predispose-to-the-genetic-variants-of-peer-reviewed-article-IJGM; https://doaj.org/toc/1178-7074

URL الوصول: https://doaj.org/article/663518cfab6d4073acaa2978ee0de942

المؤلفون: Elhawary NA; Department of Medical Genetics, College of Medicine, Umm Al-Qura University, P.O. Box 57543, Mecca, 21955, Saudi Arabia. naelhawary@uqu.edu.sa., AlJahdali IA; Department of Community Medicine, College of Medicine, Umm Al-Qura University, P.O. Box 57543, Mecca, 21955, Saudi Arabia., Abumansour IS; Department of Medical Genetics, College of Medicine, Umm Al-Qura University, P.O. Box 57543, Mecca, 21955, Saudi Arabia., Elhawary EN; Faculty of Medicine, MS Genomic Medicine Program, University of Southampton, Southampton General Hospital, Southampton, UK., Gaboon N; Department of Clinical Genetics, Faculty of Medicine, Ain Shams University, Cairo, Egypt., Dandini M; Department of Laboratory and Blood Bank, Maternity and Children Hospital, Mecca, Saudi Arabia., Madkhali A; Department of Pathology and Laboratory Medicine, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia., Alosaimi W; Department of Hematology, Maternity and Children Hospital, Mecca, Saudi Arabia., Alzahrani A; Department of Laboratory and Blood Bank at Maternity and Children Hospital, Mecca, Saudi Arabia., Aljohani F; Department of Pediatric Clinics, Maternity and Children Hospital, King Salman Medical City, Madinah, Saudi Arabia., Melibary EM; Department of Medical Genetics, College of Medicine, Umm Al-Qura University, P.O. Box 57543, Mecca, 21955, Saudi Arabia., Kensara OA; Department of Clinical Nutrition, Faculty of Applied Medical Sciences, Umm Al-Qura University, Jeddah, Saudi Arabia.; Department of Biochemistry, Batterjee Medical College, Jeddah, Saudi Arabia.

المصدر: Human genomics [Hum Genomics] 2022 Jul 19; Vol. 16 (1), pp. 22. Date of Electronic Publication: 2022 Jul 19.

نوع المنشور: Journal Article; Review; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101202210 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-7364 (Electronic) Linking ISSN: 14739542 NLM ISO Abbreviation: Hum Genomics Subsets: MEDLINE

مواضيع طبية MeSH: Phenylalanine Hydroxylase*/genetics , Phenylalanine Hydroxylase*/metabolism , Phenylalanine Hydroxylase*/therapeutic use , Phenylketonurias*/genetics , Phenylketonurias*/therapy, Humans ; Phenylalanine/metabolism ; Phenylalanine/therapeutic use