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Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.

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Title: Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.
Authors: Cerosaletti KM; Virginia Mason Research Center, University of Washington School of Medicine, Seattle, WA 98101, USA., Lange E, Stringham HM, Weemaes CM, Smeets D, Sölder B, Belohradsky BH, Taylor AM, Karnes P, Elliott A, Komatsu K, Gatti RA, Boehnke M, Concannon P
Source: American journal of human genetics [Am J Hum Genet] 1998 Jul; Vol. 63 (1), pp. 125-34.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print Cited Medium: Print ISSN: 0002-9297 (Print) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.
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  Data: <searchLink fieldCode="JN" term="%220370475%22">American journal of human genetics</searchLink> [Am J Hum Genet] 1998 Jul; Vol. 63 (1), pp. 125-34.
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  Data: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
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        Value: 10.1086/301927
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      – Code: eng
        Text: English
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        StartPage: 125
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      – TitleFull: Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.
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              Text: 1998 Jul
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              Y: 1998
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