메뉴 건너뛰기
Neurology
Volumn 48, Issue 6, 1997, Pages 1719-1721
Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17q
Author keywords

[No Author keywords available]
Indexed keywords

DNA;
EID: 0030873094     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.48.6.1719     Document Type: Article
Times cited : (25)
References (10)
  • 2
    • 0027981751 scopus 로고
    • Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies
    • Chance PF, Fischbeck KH. Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies. Hum Mol Genet 1994;3:1503-1507.
    • (1994) Hum Mol Genet , vol.3 , pp. 1503-1507
    • Chance, P.F.1    Fischbeck, K.H.2
  • 3
    • 0001215716 scopus 로고
    • Inherited recurrent focal neuropathies
    • Dyck PJ, Thomas PK, Griffin JW, Low PA, eds. Philadelphia: WB Saunders
    • Windebank AJ. Inherited recurrent focal neuropathies. In: Dyck PJ, Thomas PK, Griffin JW, Low PA, eds. Peripheral neuropathy. 3rd ed. Philadelphia: WB Saunders; 1993:1137-1148.
    • (1993) Peripheral Neuropathy. 3rd Ed. , pp. 1137-1148
    • Windebank, A.J.1
  • 4
    • 0030000575 scopus 로고    scopus 로고
    • Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17q
    • Pellegrino JE, Rebbeck TR, Brown MJ, Bird TD, Chance PF. Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17q. Neurology 1996;46:1128-1132.
    • (1996) Neurology , vol.46 , pp. 1128-1132
    • Pellegrino, J.E.1    Rebbeck, T.R.2    Brown, M.J.3    Bird, T.D.4    Chance, P.F.5
  • 5
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucl Acid Res 1988;16:1215.
    • (1988) Nucl Acid Res , vol.16 , pp. 1215
    • Miller, S.A.1    Dykes, D.D.2    Polesky, H.F.3
  • 6
    • 13344260003 scopus 로고    scopus 로고
    • Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP)
    • Timmerman V, Löfgren A, Le Guern E, et al. Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP). Hum Genet 1996;97:26-34.
    • (1996) Hum Genet , vol.97 , pp. 26-34
    • Timmerman, V.1    Löfgren, A.2    Le Guern, E.3
  • 7
    • 0031021107 scopus 로고    scopus 로고
    • Mutation analysis of the connexin 32 (Cx32) gene in Charcot-Marie-Tooth neuropathy type 1: Identification of five new mutations
    • Nelis E, Simokovic S, Timmerman V, et al. Mutation analysis of the connexin 32 (Cx32) gene in Charcot-Marie-Tooth neuropathy type 1: identification of five new mutations. Hum Mutat 1997;9:47-52.
    • (1997) Hum Mutat , vol.9 , pp. 47-52
    • Nelis, E.1    Simokovic, S.2    Timmerman, V.3
  • 8
    • 0028231090 scopus 로고
    • The 1993-94 Gênéthon human genetic linkage map
    • Gyapay G, Morissette J, Vignal A, et al. The 1993-94 Gênéthon human genetic linkage map. Nat Genet 1994;7:246-339.
    • (1994) Nat Genet , vol.7 , pp. 246-339
    • Gyapay, G.1    Morissette, J.2    Vignal, A.3
  • 10
    • 0003408936 scopus 로고
    • Baltimore and London: The Johns Hopkins University Press
    • Ott J. Analysis of human genetic linkage. Baltimore and London: The Johns Hopkins University Press, 1991.
    • (1991) Analysis of Human Genetic Linkage
    • Ott, J.1

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.