المؤلفون: Saharafi, Parisa, Akar, İrem, Ersoy-Evans, Sibel, Anlar, Banu, Varan, Ali, Vargel, Ibrahim, Cetin, Mualla, Ayter, Sukriye^{Aff1, IDs1052802310480z_cor8}

المصدر: Biochemical Genetics. 62(2):1263-1276

المؤلفون: Franciele Antonieta Bianchi Leidenz, Flavia Vasques Bittencourt, Williana Garcia Braga, Ellio Magno de Sá Araujo, Carolina Cavalieri Gomes, Vanessa de Fatima Bernardes, Eitan Friedman, Luiz De Marco

المصدر: Dermatology Practical & Conceptual, Vol 14, Iss 1 (2024)

مصطلحات موضوعية: xeroderma pigmentosum, familial melanoma, XPC, MC1R, modifier genes, Dermatology, RL1-803

وصف الملف: electronic resource

Relation: https://dpcj.org/index.php/dpc/article/view/3558; https://doaj.org/toc/2160-9381

URL الوصول: https://doaj.org/article/1d7834cca6f541a2b3f0518df49e6eb1

المؤلفون: Na Zhan, Pak C. Sham, Hon-Cheong So, Simon S. Y. Lui

المصدر: Frontiers in Genetics, Vol 14 (2023)

مصطلحات موضوعية: schizophrenia, onset age, subtyping, susceptibility genes, modifier genes, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2023.1163361/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/cbdf4695ea2d4b678b8980717c7ad4f4

المؤلفون: Rodney J. Scott

المصدر: Hereditary Cancer in Clinical Practice, Vol 20, Iss 1, Pp 1-4 (2022)

مصطلحات موضوعية: Lynch syndrome, MSH2, MLH1, Modifier genes, Incidence, Survival, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1897-4287

URL الوصول: https://doaj.org/article/b522d2a4fef046169cd1de1d3835f2c9

المؤلفون: Scott, Rodney J.^{Aff1, IDs13053022002402_cor1}

المصدر: Hereditary Cancer in Clinical Practice. 20(1)

المؤلفون: Michał Dębczyński, Giulia Gorrieri, Damian Mojsak, Floriana Guida, Federico Zara, Paolo Scudieri

المصدر: Biomolecules, Vol 13, Iss 10, p 1455 (2023)

مصطلحات موضوعية: ATP12A, modifier genes, airway acidification, cystic fibrosis, ASL, proton transport, Microbiology, QR1-502

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2218-273X/13/10/1455; https://doaj.org/toc/2218-273X

URL الوصول: https://doaj.org/article/e4fcc17ca85043fe808d9e56609ff549

المؤلفون: Gary P. Leggatt, Eleanor G. Seaby, Kristin Veighey, Christine Gast, Rodney D. Gilbert, Sarah Ennis

المصدر: Genes, Vol 14, Iss 8, p 1582 (2023)

مصطلحات موضوعية: tubulointerstitial kidney disease, genetic modifiers, modifier genes, monogenic TKD, ADTKD, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4425/14/8/1582; https://doaj.org/toc/2073-4425

URL الوصول: https://doaj.org/article/4d30d087d5764574ab48f68e17cd5794

المؤلفون: Rustam N. Mustafin

المصدر: Гений oртопедии, Vol 296, Iss 304, Pp 296-304 (2022)

مصطلحات موضوعية: modifier genes, chest deformity, neurofibromatosis type 1, pseudoarthrosis, scoliosis, Orthopedic surgery, RD701-811

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1028-4427; https://doaj.org/toc/2542-131X

URL الوصول: https://doaj.org/article/ad71bf08a59c45eb8375ec08be551669

المؤلفون: Amirifar, Parisa^{Aff1, Aff2}, Mehrmohamadi, Mahya, Ranjouri, Mohammad Reza, Akrami, Seyed Mohammad, Rezaei, Nima^{Aff2, Aff4}, Saberi, Ali, Yazdani, Reza^{Aff2, Aff4}, Abolhassani, Hassan^{Aff2, Aff6, Aff7, IDs10875021011478_cor8}, Aghamohammadi, Asghar^{Aff2, Aff8, IDs10875021011478_cor9}

المصدر: Journal of Clinical Immunology: International Journal of Inborn Errors of Immunity and Related Diseases. 42(1):72-84

المؤلفون: Hoffman, Ellen J.^Aff13112, Johnson, Kristin^Aff13113

المساهمون: Volkmar, Fred R., editor^Aff1

المصدر: Encyclopedia of Autism Spectrum Disorders. :2948-2951