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Global Medical Genetics|July 13, 2026
Genetic analysis of childhood-onset dystonia-28 caused by a variant (c.5076G>A) in the KMT2B geneWenlong Shen, Xiaopan Chen, Yajie Yuan, et al.
Global Medical Genetics|September 12, 2026
Clinical and molecular characterization of giant axonal neuropathy due to a homozygous c.851 + 1G>A variant in GAN: A case report and literature reviewEmmanuel Rojas-Morales, Eduardo Esparza-García, María Teresa Magaña-Torres
Global Medical Genetics|December 8, 2021
Impact of SARS-CoV-2 Genetic Blueprints on the Oral Manifestation of COVID-19: A Case ReportAmir Khodavirdipour, Mahsa Asadimanesh, Seyed Alireza Masoumi
Global Medical Genetics|March 22, 2021
Association of Assisted Reproductive Technology Treatments with Imprinting DisordersT Kopca, Pinar Tulay
Global Medical Genetics|March 22, 2021
CTLA-4 (+49A/G) Polymorphism in Type 1 Diabetes Children of Sudanese PopulationKhalid E Khalid Kheiralla
Global Medical Genetics|March 22, 2021
Evaluation of the Secretor Status of ABO Blood Group Antigens in Saliva using Absorption Inhibition MethodM L Avinash Tejasvi, Jaya Laksmi Bukkya, Pandu Ranga Rao, et al.
Global Medical Genetics|March 22, 2021
Association of Single Nucleotide Polymorphisms on Locus 18q21.1 in the Etiology of Nonsyndromic Cleft Lip Palate (NSCLP) in Indian Multiplex FamiliesPraveen Kumar Neela, Gosla Srinivas Reddy, Akhter Husain, et al.
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