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Annals of Human Genetics|September 8, 2022
Germline variants screening of MLH1, MSH2, MSH6 and PMS2 genes in 64 Algerian Lynch syndrome families: The first nationwide studyAsma-Lamia Boumehdi, Farid Cherbal, Feriel Khider, et al.Annals of Human Genetics|December 20, 2021
Hereditary spastic paraplegia associated with a novel homozygous intronic noncanonical splice site variant in the AP4B1 geneClara Gómez-González, Cristina Pizarro-Sánchez, Carlos Rodríguez-Antolín, et al.Annals of Human Genetics|January 1, 1986
The association of HLA-linked genes with systemic lupus erythematosusJ R Green, M Montasser, J C WoodrowAnnals of Human Genetics|July 1, 1987
Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculationsC T Falk, P RubinsteinAnnals of Human Genetics|December 10, 2021
Pseudodominant Alport syndrome caused by pathogenic homozygous and compound heterozygous COL4A3 splicing variantsMaha Mohamed, James Tellez, Carsten Bergmann, et al.Annals of Human Genetics|July 1, 1987
Localization of PEPD to the long arm of chromosome 19M B Davis, D Schonk, M Monteiro, et al.Annals of Human Genetics|November 1, 2022
High accuracy of single-molecule real-time sequencing in detecting a rare α-globin fusion gene in carrier screening populationQiao-Miao Zhou, Fan Jiang, Jing Xu, et al.Annals of Human Genetics|February 4, 2022
Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencingAshraf Yahia, Ikhlas Ben Ayed, Ahlam A Hamed, et al.Annals of Human Genetics|February 7, 2022
Role of innate immune receptors TLR4 and TLR2 polymorphisms in systemic lupus erythematosus susceptibilityNesrine Elloumi, Safa Tahri, Raouia Fakhfakh, et al.Annals of Human Genetics|April 22, 2022
A novel leaky splice variant in centromere protein J (CENPJ)-associated Seckel syndromeNavneesh Yadav, Laxmi Kirola, Thenral S Geetha, et al.Pageof 231