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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

120 related items for PubMed ID: 31355417

  • 21.
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  • 22. What primary microcephaly can tell us about brain growth.
    Cox J, Jackson AP, Bond J, Woods CG.
    Trends Mol Med; 2006 Aug; 12(8):358-66. PubMed ID: 16829198
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  • 26. Congenital cystic microphthalmia and consequent anophthalmia in the rat: a study in abnormal ocular morphogenesis.
    Kinney HC, Klintworth GK, Lesiewicz J, Goldsmith LA, Wilkening B.
    Teratology; 1982 Oct; 26(2):203-12. PubMed ID: 7157196
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  • 27. Confirmation of TENM3 involvement in autosomal recessive colobomatous microphthalmia.
    Chassaing N, Ragge N, Plaisancié J, Patat O, Geneviève D, Rivier F, Malrieu-Eliaou C, Hamel C, Kaplan J, Calvas P.
    Am J Med Genet A; 2016 Jul; 170(7):1895-8. PubMed ID: 27103084
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  • 28. A novel nonsense CDK5RAP2 mutation in a Somali child with primary microcephaly and sensorineural hearing loss.
    Pagnamenta AT, Murray JE, Yoon G, Sadighi Akha E, Harrison V, Bicknell LS, Ajilogba K, Stewart H, Kini U, Taylor JC, Keays DA, Jackson AP, Knight SJ.
    Am J Med Genet A; 2012 Oct; 158A(10):2577-82. PubMed ID: 22887808
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  • 30. Human microcephaly ASPM protein is a spindle pole-focusing factor that functions redundantly with CDK5RAP2.
    Tungadi EA, Ito A, Kiyomitsu T, Goshima G.
    J Cell Sci; 2017 Nov 01; 130(21):3676-3684. PubMed ID: 28883092
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  • 31. Compound heterozygote CDK5RAP2 mutations in a Guatemalan/Honduran child with autosomal recessive primary microcephaly, failure to thrive and speech delay.
    Li MH, Arndt K, Das S, Weiss EM, Wu Y, Gwal K, Shekdar KV, Zackai EH.
    Am J Med Genet A; 2015 Jun 01; 167(6):1414-7. PubMed ID: 25899944
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  • 33. Eye anomalies: seasonal variation and maternal viral infections.
    Busby A, Dolk H, Armstrong B.
    Epidemiology; 2005 May 01; 16(3):317-22. PubMed ID: 15824546
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  • 36. Genetics of microphthalmos.
    Warburg M.
    Int Ophthalmol; 1981 Aug 01; 4(1-2):45-65. PubMed ID: 6795139
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  • 37. Microphthalmia and associated abnormalities in inbred black mice.
    Smith RS, Roderick TH, Sundberg JP.
    Lab Anim Sci; 1994 Dec 01; 44(6):551-60. PubMed ID: 7898027
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  • 38. Anophthalmia-microphthalmia-oblique clefting syndrome: confirmation of the Fryns anophthalmia syndrome.
    Warburg M, Jensen H, Prause JU, Bolund S, Skovby F, Miranda MJ.
    Am J Med Genet; 1997 Nov 28; 73(1):36-40. PubMed ID: 9375920
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  • 40. A novel heterozygous SOX2 mutation causing anophthalmia/microphthalmia with genital anomalies.
    Pedace L, Castori M, Binni F, Pingi A, Grammatico B, Scommegna S, Majore S, Grammatico P.
    Eur J Med Genet; 2009 Nov 28; 52(4):273-6. PubMed ID: 19254784
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