Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Syndrome and PCNT[original query] |
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Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation. American journal of medical genetics. Part A 2020 4 182 (6): 1407-1420. Abdel-Salam Ghada M H, Sayed Inas S M, Afifi Hanan H, Abdel-Ghafar Sherif F, Abouzaid Maha R, Ismail Samira I, Aglan Mona S, Issa Mahmoud Y, El-Bassyouni Hala T, El-Kamah Ghada, Effat Laila K, Eid Maha, Zaki Maha S, Temtamy Samia A, Abdel-Hamid Mohamed |
Family-Based Analysis Combined with Case-Controls Study Implicate Roles of PCNT in Tourette Syndrome. Neuropsychiatric disease and treatment 2020 16 349-354. Liu Wenmiao, Guo Yixia, Liu Xiumei, Zhang Ru, Dong Jicheng, Deng Hao, He Fan, Che Fengyuan, Liu Shiguo, Yi Ming |
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