An anonymous single copy X-chromosome clone DXS91, from Xq11-q13, identifies a moderately frequent RFLP.
作者信息
Davatelis G, Siniscalco M, Szabo P
出版信息
Nucleic Acids Res. 1985 Oct 25;13(20):7539. doi: 10.1093/nar/13.20.7539.
Abstract
摘要
相似文献
1
An anonymous single copy X-chromosome clone DXS91, from Xq11-q13, identifies a moderately frequent RFLP.
Nucleic Acids Res. 1985 Oct 25;13(20):7539. doi: 10.1093/nar/13.20.7539.
2
An anonymous single copy X-chromosome clone DXS92, from Xq26-27, identifies two frequent RFLPs.
Nucleic Acids Res. 1985 Oct 25;13(20):7540. doi: 10.1093/nar/13.20.7540.
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An anonymous single copy X-chromosome clone, pTAK8, identifies a frequent RFLP at Xp11-q12(HGM8 no. DXS146).
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4
An anonymous single copy X-chromosome clone DXS94 from Xq11-q21 identifies a common RFLP.
Nucleic Acids Res. 1987 Jun 11;15(11):4694. doi: 10.1093/nar/15.11.4694.
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An anonymous human single copy genomic clone, D11S29 (L7) at 11q23, identifies a moderately frequent RFLP.
Nucleic Acids Res. 1986 Feb 25;14(4):1920. doi: 10.1093/nar/14.4.1920.
6
An anonymous human single copy genomic clone (D8S5) (TL11) on chromosome 8 identifies a moderately frequent RFLP.
Nucleic Acids Res. 1986 Aug 26;14(16):6781. doi: 10.1093/nar/14.16.6781.
7
An anonymous single-copy clone, p30-1-60, identifies a frequent RFLP on chromosome 3p [HGM9 no. D3S86].
Nucleic Acids Res. 1989 Apr 11;17(7):2883. doi: 10.1093/nar/17.7.2883.
8
Single copy X-chromosome clone p8 from Xq11-Xq13 identifies further low frequency RFLP [HGM8 no. DXS1].
Nucleic Acids Res. 1987 Jun 11;15(11):4695. doi: 10.1093/nar/15.11.4695.
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An anonymous single copy genomic clone (M8) (D2S13) on chromosome 2 identifies a moderately frequent RFLP.
Nucleic Acids Res. 1986 Aug 26;14(16):6780. doi: 10.1093/nar/14.16.6780.
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An anonymous single copy chromosome 22 clone, D22S10 (22c1-18) identifies an RFLP with PstI.
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Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.I.
Am J Hum Genet. 1990 Jul;47(1):20-7.
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