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1دورية أكاديمية
المؤلفون: Naveed Muhammad, Abid Amina, Aziz Tariq, Saleem Ayesha, Hanif Nimra, Ali Imran, Alasmari Abdullah F.
المصدر: Open Chemistry, Vol 22, Iss 1, Pp 66-71 (2024)
مصطلحات موضوعية: epibulbar dermoid cyst, ptch1 gene, fisetin, computational ai-based drug, Chemistry, QD1-999
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2391-5420
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2دورية أكاديمية
المؤلفون: Hyo Seong Kim, Seung Heo, Kyung Sik Kim, Joon Choi, Jeong Yeol Yang
المصدر: Archives of Plastic Surgery, Vol 50, Iss 04, Pp 384-388 (2023)
مصطلحات موضوعية: Gorlin–Goltz syndrome, PTCH1 gene, basal cell carcinoma syndrome, Surgery, RD1-811
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: QingQing Deng, Yan Li, ZhanLi Liu, JieLin Zhou, LingWei Weng
المصدر: Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-5 (2022)
مصطلحات موضوعية: Epidermal nevus syndrome, PTCH1 gene, Cerebral infarction, Paralysis, Cerebrovascular malformation, Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1752-1947
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4دورية أكاديمية
المؤلفون: Deng, QingQingAff1, IDs13256022035479_cor1, Li, Yan, Liu, ZhanLi, Zhou, JieLin, Weng, LingWei
المصدر: Journal of Medical Case Reports. 16(1)
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5دورية أكاديمية
المؤلفون: Zhou, JunfengAff1, Aff2, Zhang, Guiying, Shi, Meng, Liu, Zhisheng, Xiao, Manyi, Fu, Siqi, Gong, Xiaoyan, Shi, XiaoliuAff1, Aff2
المصدر: Medical Molecular Morphology. 52(4):235-237
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6دورية أكاديمية
المؤلفون: Gozde Ozcan, Burhan Balta, Ahmet Ercan Sekerci, Osman A Etoz, Claudia Martinuzzi, Ozlem Kara, Lorenza Pastorino, Fatma Kocoglu, Omer Ulker, Murat Erdogan
المصدر: Indian Journal of Pathology and Microbiology, Vol 59, Iss 3, Pp 335-338 (2016)
مصطلحات موضوعية: Gorlin–Goltz syndrome, nevoid basal cell nevus syndrome, odontogenic keratocyst, pediatric, PTCH1 gene, Pathology, RB1-214, Microbiology, QR1-502
وصف الملف: electronic resource
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7
المؤلفون: Gulibaha Maimaitili, Jiuxiang Lin, Huizhe Huang, Chong Chen, Huaxiang Zhao, Zulihumaer Nueraihemaiti, Wenbin Huang, Wenjie Zhong, Dilifeire Tuerhong, Yue Zhang, Feng Chen, Qian Zhang, Mengqi Zhang
المصدر: Genes and Diseases, Vol 8, Iss 5, Pp 689-697 (2021)
مصطلحات موضوعية: 0301 basic medicine, Patched, Medicine (General), endocrine system, PTCH1, QH426-470, Biology, medicine.disease_cause, Biochemistry, 03 medical and health sciences, R5-920, 0302 clinical medicine, Genetics, medicine, Clinical genetics, Molecular Biology, Gene, Genetics (clinical), Exome sequencing, Genotype-phenotype analysis, Mutation, Cell Biology, PTCH1 Gene, Phenotype, Penetrance, Cleft lip with or without palate, 030104 developmental biology, Whole-exome sequencing, 030220 oncology & carcinogenesis
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8دورية أكاديمية
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9كتاب إلكتروني
المؤلفون: Chrzanowska, Krystyna H.Aff3, Trubicka, JoannaAff3, Ciara, ElżbietaAff3
المساهمون: Hayat, M. A., Series editorAff1, Hayat, M.A., editorAff2
المصدر: Pediatric Cancer, Volume 3 : Diagnosis, Therapy, and Prognosis. 3:117-127
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10
المؤلفون: Michael Sharkey, Adam D. Ewing, Richard Walker, Seth W. Cheetham, Malcolm J. West, Kim M. Summers, James J McGill, Jennifer West
المصدر: American Journal of Medical Genetics. Part a
مصطلحات موضوعية: 0301 basic medicine, Male, PTCH1, Adolescent, Basal Cell Nevus Syndrome, Chromosome 9, Chromosome Disorders, 030105 genetics & heredity, Biology, Severity of Illness Index, 03 medical and health sciences, 9q22.3 deletion, Genetics, Humans, Genetic Predisposition to Disease, Child, Gene, Genetics (clinical), Point mutation, Fanconi Anemia Complementation Group C Protein, DNA Helicases, Infant, Newborn, Chromosome, Infant, PTCH1 Gene, Original Articles, Phenotype, Gorlin syndrome, Patched-1 Receptor, 030104 developmental biology, Child, Preschool, Odontogenic Cysts, Original Article, Neoplasm Recurrence, Local, Chromosomes, Human, Pair 9