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Journal Abstract Search

118 related items for PubMed ID: 34693918

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  • 5. Molecular genetic analysis of consanguineous families with primary microcephaly identified pathogenic variants in the ASPM gene.
    Khan MA, Windpassinger C, Ali MZ, Zubair M, Gul H, Abbas S, Khan S, Badar M, Mohammad RM, Nawaz Z.
    J Genet; 2017 Jun; 96(2):383-387. PubMed ID: 28674240
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  • 7. Microcephaly primary hereditary (MCPH): Report of novel ASPM variants and prenatal diagnosis in a Vietnamese family.
    Tran TH, Diep QM, Cao MH, Luong LH, Pham VA, Lan Dinh OT, Bui TH, Van Ta T, Tran VK.
    Taiwan J Obstet Gynecol; 2021 Sep; 60(5):907-910. PubMed ID: 34507672
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  • 10. ASPM mutations identified in patients with primary microcephaly and seizures.
    Shen J, Eyaid W, Mochida GH, Al-Moayyad F, Bodell A, Woods CG, Walsh CA.
    J Med Genet; 2005 Sep; 42(9):725-9. PubMed ID: 16141009
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  • 11. Novel Pathogenic Mutation Mapping of ASPM Gene in Consanguineous Pakistani Families with Primary Microcephaly.
    Batool T, Irshad S, Mahmood K.
    Braz J Biol; 2021 Sep; 83():e246040. PubMed ID: 34378666
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  • 12. A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family.
    Naseer MI, Rasool M, Sogaty S, Chaudhary RA, Mansour HM, Chaudhary AG, Abuzenadah AM, Al-Qahtani MH.
    Ann Saudi Med; 2017 Sep; 37(2):148-153. PubMed ID: 28377545
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  • 13. A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephaly.
    Hashmi JA, Al-Harbi KM, Ramzan K, Albalawi AM, Mehmood A, Samman MI, Basit S.
    Ann Saudi Med; 2016 Sep; 36(6):391-396. PubMed ID: 27920410
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