Human Genome Epidemiology Literature Finder

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Records 1 - 5 (of 5 Records)

Query Trace: Disease and GTF2H2[original query]
A population-based study of genotypic and phenotypic variability in children with spinal muscular atrophy. Acta paediatrica (Oslo, Norway : 1992) 2009 May 98 (5): 865-72. Arkblad Eva, Tulinius Már, Kroksmark Anna-Karin, Henricsson Mirja, Darin Nikl Similar articles in PubMed
[Analysis and carrier screening for copy numbers of SMN and NAIP genes in children with spinal muscular atrophy]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2014 Apr 31 (2): 152-5. Zeng Guangqun, Zheng Hong, Cheng Jing, Chen Rong, Lin He, Yang Jiyun, Zhang Dingdi Similar articles in PubMed
Genetic findings of Cypriot spinal muscular atrophy patients. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Oct 36 (10): 1829-34. Theodorou L, Nicolaou P, Koutsou P, Georghiou A, Anastasiadou V, Tanteles G, Kyriakides T, Zamba-Papanicolaou E, Christodoulou Similar articles in PubMed
Whole Exome Sequencing Study of Parkinson Disease and Related Endophenotypes in the Italian Population. Frontiers in neurology 2019 10 1362. Gialluisi Alessandro, Reccia Mafalda Giovanna, Tirozzi Alfonsina, Nutile Teresa, Lombardi Alessia, De Sanctis Claudia, , Varanese Sara, Pietracupa Sara, Modugno Nicola, Simeone Antonio, Ciullo Marina, Esposito Tere Similar articles in PubMed
Molecular analysis of SMN2, NAIP, and GTF2H2 gene deletions and relationships with clinical subtypes of spinal muscular atrophy. Journal of neurogenetics 2024 9 1-10. Nilgun Karasu, Hamit Acer, Hilal Akalin, Burcu Turkgenc, Mikail Demir, Izem Olcay Sahin, Nuriye Gokce, Ayten Gulec, Asli Ciplakligil, Ayse Caglar Sarilar, Isa Cuce, Hakan Gumus, Huseyin Per, Mehmet Canpolat, Munis Dund Similar articles in PubMed