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Journal Abstract Search

335 related items for PubMed ID: 8154871

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  • 8. 16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study.
    Ouyang Y, Sakoe K, Shimazaki H, Namekawa M, Ogawa T, Ando Y, Kawakami T, Kaneko J, Hasegawa Y, Yoshizawa K, Amino T, Ishikawa K, Mizusawa H, Nakano I, Takiyama Y.
    J Neurol Sci; 2006 Sep 25; 247(2):180-6. PubMed ID: 16780885
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  • 9. Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1.
    Jöbsis GJ, Weber JW, Barth PG, Keizers H, Baas F, van Schooneveld MJ, van Hilten JJ, Troost D, Geesink HH, Bolhuis PA.
    J Neurol Neurosurg Psychiatry; 1997 Apr 25; 62(4):367-71. PubMed ID: 9120450
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  • 10. [Clinico-genetic study of type I spinocerebelllar ataxia].
    Svetel M, Culjković B, Sternić N, Dragasević B, Stojković I, Romac S, Kostić VS.
    Srp Arh Celok Lek; 1999 Apr 25; 127(5-6):157-62. PubMed ID: 10500422
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  • 11. SCA2 is not a major locus for ADCA type I in French families.
    Cancel G, Stevanin G, Dürr A, Chneiweiss H, Penet C, Pothin Y, Agid Y, Brice A.
    Am J Med Genet; 1995 Oct 09; 60(5):382-5. PubMed ID: 8546150
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  • 14. Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan.
    Li M, Ishikawa K, Toru S, Tomimitsu H, Takashima M, Goto J, Takiyama Y, Sasaki H, Imoto I, Inazawa J, Toda T, Kanazawa I, Mizusawa H.
    J Hum Genet; 2003 Oct 09; 48(3):111-8. PubMed ID: 12624721
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  • 15. Autosomal dominant cerebellar ataxia type I linked to chromosome 12q (SCA2: spinocerebellar ataxia type 2).
    Dürr A, Brice A, Lepage-Lezin A, Cancel G, Smadja D, Vernant JC, Agid Y.
    Clin Neurosci; 1995 Oct 09; 3(1):12-6. PubMed ID: 7614088
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  • 16. A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan.
    Takashima M, Ishikawa K, Nagaoka U, Shoji S, Mizusawa H.
    J Hum Genet; 2001 Oct 09; 46(4):167-71. PubMed ID: 11322654
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  • 18. Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3.
    Olsson JE, Samanns C, Jimenez J, Pongratz J, Chand A, Watty A, Seuchter SA, Denton M, Gal A.
    Am J Med Genet; 1990 Apr 09; 35(4):595-9. PubMed ID: 2333895
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