Literature DB >> 2446265

MspI RFLP detected with chromosome-walk clone pXUT23-SE3.2L from DXS16 in Xp22.1-22.3.

C J Brown1, H F Willard.   

Abstract

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Year:  1987        PMID： 2446265      PMCID： PMC306506          DOI： 10.1093/nar/15.22.9614

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


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  1 in total

1.  Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs.

Authors:  E Bakker; M H Hofker; N Goor; J L Mandel; K Wrogemann; K E Davies; L M Kunkel; H F Willard; W A Fenton; L Sandkuyl
Journal:  Lancet       Date:  1985-03-23       Impact factor: 79.321
  1 in total
  3 in total

1.  Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome.

Authors:  C J Brown; M M Mahtani; H F Willard
Journal:  Hum Genet       Date:  1988-11       Impact factor: 4.132

2.  Regional localization of the TIMP gene on the human X chromosome. Extension of a conserved synteny and linkage group on proximal Xp.

Authors:  H F Willard; S J Durfy; M M Mahtani; H Dorkins; K E Davies; B R Williams
Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

3.  Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes.

Authors:  P A Sieving; E L Bingham; M S Roth; M R Young; M Boehnke; C Y Kuo; D Ginsburg
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025
  3 in total

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