Literature DB >> 2566968

XmnI polymorphism of the human STS gene.

B Wirth1, A Gal.   

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Year:  1989        PMID： 2566968      PMCID： PMC317765          DOI： 10.1093/nar/17.8.3326

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


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  5 in total

1.  Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type.

Authors:  A A Bergen; C Samanns; E J Schuurman; L van Osch; D B van Dorp; A J Pinckers; E Bakker; A Gal; G J van Ommen; E M Bleeker-Wagemakers
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

2.  Molecular analysis of aberrations of Xp and Yq.

Authors:  S D Cheng; R Gasparini; U Müller
Journal:  Hum Genet       Date:  1992-02       Impact factor: 4.132

3.  A multipoint linkage map of the distal short arm of the human X chromosome.

Authors:  C L Johnson; P Charmley; P H Yen; L J Shapiro
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

4.  An NcoI restriction fragment length polymorphism at the human steroid sulphatase gene locus.

Authors:  P M van Zandvoort; C A van Bennekom; H H Ropers; B A van Oost
Journal:  Hum Genet       Date:  1990-04       Impact factor: 4.132

5.  Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.

Authors:  T Meitinger; B Heye; C Petit; J Levilliers; A Golla; C Moraine; B Dalla Piccola; W G Sippell; J Murken; A Ballabio
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025
  5 in total

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