Literature DB >> 1923839

Tetranucleotide repeat polymorphism at the HPRT locus.

C M Hearne1, J A Todd.   

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Year:  1991        PMID: 1923839      PMCID: PMC328931     

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


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  3 in total

1.  Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms.

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2.  Automated DNA sequencing of the human HPRT locus.

Authors:  A Edwards; H Voss; P Rice; A Civitello; J Stegemann; C Schwager; J Zimmermann; H Erfle; C T Caskey; W Ansorge
Journal:  Genomics       Date:  1990-04       Impact factor: 5.736

3.  Towards construction of a high resolution map of the mouse genome using PCR-analysed microsatellites.

Authors:  J M Love; A M Knight; M A McAleer; J A Todd
Journal:  Nucleic Acids Res       Date:  1990-07-25       Impact factor: 16.971

  3 in total
  11 in total

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Review 2.  Use of X-linked markers for forensic purposes.

Authors:  R Szibor; M Krawczak; S Hering; J Edelmann; E Kuhlisch; D Krause
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3.  Nomenclature discrepancies in the HPRTB short tandem repeat.

Authors:  Reinhard Szibor; Jeanett Edelmann; Sandra Hering; Iva Gomes; Leonor Gusmão
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4.  X chromosomal recombination--a family study analysing 39 STR markers in German three-generation pedigrees.

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5.  X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

Authors:  M Lagerström-Fermér; M Sundvall; E Johnsen; G L Warne; S M Forrest; J D Zajac; A Rickards; D Ravine; U Landegren; U Pettersson
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

6.  Genetic polymorphisms and mutation rates of 16 X-STRs in a Han Chinese population of Beijing and application examples in second-degree kinship cases.

Authors:  Man Chen; He Ren; Zhiyong Liu; Jing Zhao; Chong Chen; Yan Shi; Li Jia; Feng Cheng; Tong Chen; Qingwei Fan; Yaran Yang; Yacheng Liu; Gengqian Zhang; Jiangwei Yan
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7.  Linkage mapping of a severe X-linked mental retardation syndrome.

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8.  Evaluation of 13 short tandem repeat loci for use in personal identification applications.

Authors:  H A Hammond; L Jin; Y Zhong; C T Caskey; R Chakraborty
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9.  Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family.

Authors:  F A Hol; M P Geurds; O Jensson; B C Hamel; G E Moore; R Newton; E C Mariman
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10.  Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.

Authors:  S J Scheinman; M A Pook; C Wooding; J T Pang; P A Frymoyer; R V Thakker
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