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Journal Abstract Search

223 related items for PubMed ID: 25232855

  • 1. Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disability.
    Gandin I, Faletra F, Faletra F, Carella M, Pecile V, Ferrero GB, Biamino E, Palumbo P, Palumbo O, Bosco P, Romano C, Belcaro C, Vozzi D, d'Adamo AP.
    Genet Med; 2015 May; 17(5):396-9. PubMed ID: 25232855
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  • 3. Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families.
    Moudi M, Vahidi Mehrjardi MY, Hozhabri H, Metanat Z, Kalantar SM, Taheri M, Ghasemi N, Dehghani M.
    J Clin Lab Anal; 2022 Feb; 36(2):e24241. PubMed ID: 35019165
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  • 4. Homozygosity mapping of autosomal recessive intellectual disability loci in 11 consanguineous Pakistani families.
    Ahmed I, Rafiq MA, Vincent JB, Bhatti A, Ayub M, John P.
    Acta Neuropsychiatr; 2015 Feb; 27(1):38-47. PubMed ID: 25434728
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  • 5. Effect of inbreeding on intellectual disability revisited by trio sequencing.
    Kahrizi K, Hu H, Hosseini M, Kalscheuer VM, Fattahi Z, Beheshtian M, Suckow V, Mohseni M, Lipkowitz B, Mehvari S, Mehrjoo Z, Akhtarkhavari T, Ghaderi Z, Rahimi M, Arzhangi S, Jamali P, Falahat Chian M, Nikuei P, Sabbagh Kermani F, Sadeghinia F, Jazayeri R, Tonekaboni SH, Khoshaeen A, Habibi H, Pourfatemi F, Mojahedi F, Khodaie-Ardakani MR, Najafipour R, Wienker TF, Najmabadi H, Ropers HH.
    Clin Genet; 2019 Jan; 95(1):151-159. PubMed ID: 30315573
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  • 6. Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family.
    Chograni M, Alkuraya FS, Ourteni I, Maazoul F, Lariani I, Chaabouni HB.
    Clin Genet; 2015 Sep; 88(3):283-7. PubMed ID: 25358429
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  • 7. Genetics of recessive cognitive disorders.
    Musante L, Ropers HH.
    Trends Genet; 2014 Jan; 30(1):32-9. PubMed ID: 24176302
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  • 9. A novel variant of C12orf4 in a consanguineous Armenian family confirms the etiology of autosomal recessive intellectual disability type 66 with delineation of the phenotype.
    Hancarova M, Babikyan D, Bendova S, Midyan S, Prchalova D, Shahsuvaryan G, Stranecky V, Sarkisian T, Sedlacek Z.
    Mol Genet Genomic Med; 2019 Sep; 7(9):e865. PubMed ID: 31334606
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  • 15. Fine mapping of MRT9 locus through genome wide homozygosity mapping in a consanguineous Pakistani family.
    Rehman SU, Baig SM, Hasen L, Ahmad I, Khan RA, Hussa M.
    J Pak Med Assoc; 2019 Dec; 69(12):1903-1906. PubMed ID: 31853126
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  • 16. Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity.
    Abou Jamra R, Wohlfart S, Zweier M, Uebe S, Priebe L, Ekici A, Giesebrecht S, Abboud A, Al Khateeb MA, Fakher M, Hamdan S, Ismael A, Muhammad S, Nöthen MM, Schumacher J, Reis A.
    Eur J Hum Genet; 2011 Nov; 19(11):1161-6. PubMed ID: 21629298
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  • 17. Advances in identification of genes involved in autosomal recessive intellectual disability: a brief review.
    Mir YR, Kuchay RAH.
    J Med Genet; 2019 Sep; 56(9):567-573. PubMed ID: 30842223
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  • 18. Next Generation Sequencing and Genome-Wide Genotyping Identify the Genetic Causes of Intellectual Disability in Ten Consanguineous Families from Jordan.
    Froukh TJ.
    Tohoku J Exp Med; 2017 Dec; 243(4):297-309. PubMed ID: 29269699
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