Literature DB >> 4041033

An anonymous single-copy X-chromosome RFLP for DXS72 from Xq13-Xq22 [HGM8 provisional no. DXS72].

B J Schmeckpeper, J Davis, H F Willard, K D Smith.   

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Year:  1985        PMID： 4041033      PMCID： PMC321903          DOI： 10.1093/nar/13.15.5724

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


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  1 in total

1.  Isolation and characterization of cloned human DNA fragments carrying reiterated sequences common to both autosomes and the X chromosome.

Authors:  B J Schmeckpeper; H F Willard; K D Smith
Journal:  Nucleic Acids Res       Date:  1981-04-24       Impact factor: 16.971
  1 in total
  6 in total

1.  Alport syndrome: a genetic study of 31 families.

Authors:  R M'Rad; M Sanak; G Deschenes; J Zhou; C Bonaiti-Pellie; L Holvoet-Vermaut; S Heuertz; M C Gubler; M Broyer; J P Grunfeld
Journal:  Hum Genet       Date:  1992-12       Impact factor: 4.132

2.  Dystonia-parkinsonism syndrome (XDP) locus: flanking markers in Xq12-q21.1.

Authors:  K G Kupke; M B Graeber; U Müller
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

3.  Lowe oculocerebrorenal syndrome: DNA-based linkage of the gene to Xq24-q26, using tightly linked flanking markers and the correlation to lens examination in carrier diagnosis.

Authors:  C Wadelius; P Fagerholm; U Pettersson; G Annerén
Journal:  Am J Hum Genet       Date:  1989-02       Impact factor: 11.025

4.  Haplotype and multipoint linkage analysis in Finnish choroideremia families.

Authors:  E M Sankila; T Lehner; A W Eriksson; H Forsius; J Kärnä; D Page; J Ott; A de la Chapelle
Journal:  Hum Genet       Date:  1989-12       Impact factor: 4.132

5.  X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.

Authors:  J Zonana; A Clarke; M Sarfarazi; N S Thomas; K Roberts; K Marymee; P S Harper
Journal:  Am J Hum Genet       Date:  1988-07       Impact factor: 11.025

6.  Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.

Authors:  J G Lesko; R A Lewis; R L Nussbaum
Journal:  Am J Hum Genet       Date:  1987-04       Impact factor: 11.025
  6 in total

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