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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

223 related items for PubMed ID: 20301582

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    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Angelini C.
    ; 1993. PubMed ID: 20301490
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  • 4. Molecular Diagnosis of Limb-Girdle Muscular Dystrophy Using Next-Generation Sequencing Panels.
    Sarıkaya Uzan G, Yılmaz Uzman C, Çinleti T, Günay Ç, Ülgenalp A, Hız Kurul S, Yiş U.
    Mol Syndromol; 2024 Feb; 15(1):14-21. PubMed ID: 38357257
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    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Bruno C, Sotgia F, Gazzerro E, Minetti C, Lisanti MP.
    ; 1993 Feb. PubMed ID: 20301559
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  • 9. Molecular bases of autosomal recessive limb-girdle muscular dystrophies.
    Nigro V.
    Acta Myol; 2003 Sep; 22(2):35-42. PubMed ID: 14959561
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  • 10. Clinical, pathological, imaging, and genetic characterization in a Taiwanese cohort with limb-girdle muscular dystrophy.
    Liang WC, Jong YJ, Wang CH, Wang CH, Tian X, Chen WZ, Kan TM, Minami N, Nishino I, Wong LC.
    Orphanet J Rare Dis; 2020 Jun 23; 15(1):160. PubMed ID: 32576226
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  • 14. Elucidation of the Genetic Cause in Dutch Limb Girdle Muscular Dystrophy Families: A 27-Year's Journey.
    Ten Dam L, de Visser M, Ginjaar IB, van Duyvenvoorde HA, van Koningsbruggen S, van der Kooi AJ.
    J Neuromuscul Dis; 2021 Jun 23; 8(2):261-272. PubMed ID: 33386810
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  • 15.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Foley AR, Mohassel P, Donkervoort S, Bolduc V, Bönnemann CG.
    ; 1993 Jun 23. PubMed ID: 20301676
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  • 16. Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD study.
    Doody A, Alfano L, Diaz-Manera J, Lowes L, Mozaffar T, Mathews KD, Weihl CC, Wicklund M, Hung M, Statland J, Johnson NE, GRASP-LGMD Consortium.
    BMC Neurol; 2024 Mar 15; 24(1):96. PubMed ID: 38491364
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  • 17. Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients.
    Ten Dam L, Frankhuizen WS, Linssen WHJP, Straathof CS, Niks EH, Faber K, Fock A, Kuks JB, Brusse E, de Coo R, Voermans N, Verrips A, Hoogendijk JE, van der Pol L, Westra D, de Visser M, van der Kooi AJ, Ginjaar I.
    Clin Genet; 2019 Aug 15; 96(2):126-133. PubMed ID: 30919934
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  • 18. The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease.
    Bevilacqua JA, Guecaimburu Ehuletche MDR, Perna A, Dubrovsky A, Franca MC, Vargas S, Hegde M, Claeys KG, Straub V, Daba N, Faria R, Periquet M, Sparks S, Thibault N, Araujo R.
    Orphanet J Rare Dis; 2020 Jan 13; 15(1):11. PubMed ID: 31931849
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  • 19. Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients.
    Lin F, Yang K, Lin X, Jin M, Chen L, Zheng FZ, Qiu LL, Ye ZX, Chen HZ, Lin MT, Wang N, Wang ZQ.
    Orphanet J Rare Dis; 2023 Nov 16; 18(1):356. PubMed ID: 37974208
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  • 20.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Bonne G, Leturcq F, Ben Yaou R.
    ; 1993 Nov 16. PubMed ID: 20301609
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