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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

205 related items for PubMed ID: 10586280

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  • 26. Prenatal detection of a 17p11.2 duplication resulting from a rare recombination event and novel PCR-based strategy for molecular identification of Charcot-Marie-Tooth disease type 1A.
    Bernard R, Labelle V, Negre P, Tardieu S, Azulay JP, Malzac P, Mattéi JF, Leguern E, Philip N, Lévy N.
    Eur J Hum Genet; 2000 Mar; 8(3):229-35. PubMed ID: 10780790
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  • 29. Neurophysiology and molecular genetics of Charcot-Marie-Tooth type 1 neuropathy in Croatian children: follow-up study.
    Barisić N, Mihatov I.
    Croat Med J; 2000 Sep; 41(3):306-13. PubMed ID: 10962051
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  • 30. A patient with both Charcot-Marie-Tooth disease (CMT 1A) and mild spinal muscular atrophy (SMA 3).
    Jedrzejowska M, Ryniewicz B, Kabzińska D, Drac H, Hausmanowa-Petrusewicz I, Kochański A.
    Neuromuscul Disord; 2008 Apr; 18(4):339-41. PubMed ID: 18337101
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  • 31. [Study of the duplication of 17p11.2-12 chromosome region in the patients with hereditary motor and sensory neuropathy type 1A].
    Hryshchenko NV, Bychkova AM, Pichkur NA, Skyban HV, Dmytrenko VV, Livshyts' LA.
    Tsitol Genet; 2003 Apr; 37(6):55-9. PubMed ID: 15067947
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  • 36. Severe phenotype with cis-acting heterozygous PMP22 mutations.
    Niedrist D, Joncourt F, Mátyás G, Müller A.
    Clin Genet; 2009 Mar; 75(3):286-9. PubMed ID: 19067730
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  • 39. Human nerve pathology caused by different mutational mechanisms of the PMP22 gene.
    Gabreëls-Festen A, Wetering RV.
    Ann N Y Acad Sci; 1999 Sep 14; 883():336-43. PubMed ID: 10586258
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