A deleterious frameshift insertion mutation in the <i>ZNF142</i> gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature reviewAtefeh Mir, Mohammad Amin Tabatabaiefar, Yongjun Song et al.|Molecular Genetics & Genomic Medicine|2023Cited by 8
Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literatureAtefeh Mir, Mohammad Amin Tabatabaiefar, Yongjun Song et al.|BMC Medical Genomics|2023Cited by 6
A novel de novo frameshift variant in the <scp><i>CHD2</i></scp> gene related to intellectual and developmental disability, seizures and speech problemsAtefeh Mir, Mohammad Amin Tabatabaiefar, Yongjun Song et al.|Molecular Genetics & Genomic Medicine|2023Cited by 1
Correction: whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literatureAtefeh Mir, Mohammad Amin Tabatabaiefar, Erfan Khorram et al.|BMC Medical Genomics|2025Cited by 0
Identification of Xq22.1-23 as a region linked with hereditary recurrent spontaneous abortion in a family.Sahar Shekouhi, Majid Mojarrad, Mohammad Amin Tabatabaiefar et al.|PubMed|2013Cited by 0