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Journal Abstract Search

129 related items for PubMed ID: 24321734

  • 1. A simplified approach for FSHD molecular testing.
    Papanikos F, Skoulatou C, Sakellariou P, Kekou K, Christopoulos TK, Kanavakis E, Traeger-Synodinos J, Ioannou PC.
    Clin Chim Acta; 2014 Feb 15; 429():96-103. PubMed ID: 24321734
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  • 6. Distinguishing the 4qA and 4qB variants is essential for the diagnosis of facioscapulohumeral muscular dystrophy in the Chinese population.
    Wang ZQ, Wang N, van der Maarel S, Murong SX, Wu ZY.
    Eur J Hum Genet; 2011 Jan 15; 19(1):64-9. PubMed ID: 20736973
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  • 8. D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detection.
    Lemmers RJ, Osborn M, Haaf T, Rogers M, Frants RR, Padberg GW, Cooper DN, van der Maarel SM, Upadhyaya M.
    Neurology; 2003 Jul 22; 61(2):178-83. PubMed ID: 12874395
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  • 11. Worldwide population analysis of the 4q and 10q subtelomeres identifies only four discrete interchromosomal sequence transfers in human evolution.
    Lemmers RJ, van der Vliet PJ, van der Gaag KJ, Zuniga S, Frants RR, de Knijff P, van der Maarel SM.
    Am J Hum Genet; 2010 Mar 12; 86(3):364-77. PubMed ID: 20206332
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  • 12. Single-molecule optical mapping enables quantitative measurement of D4Z4 repeats in facioscapulohumeral muscular dystrophy (FSHD).
    Dai Y, Li P, Wang Z, Liang F, Yang F, Fang L, Huang Y, Huang S, Zhou J, Wang D, Cui L, Wang K.
    J Med Genet; 2020 Feb 12; 57(2):109-120. PubMed ID: 31506324
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