Literature DB >> 4017373

[Duchenne muscular dystrophy in a female with an X-autosome translocation].

O Narazaki, T Hanai, Y Ueki, A Mitsudome.   

Abstract

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Year:  1985        PMID： 4017373

Source DB:  PubMed          Journal:  Rinsho Shinkeigaku        ISSN： 0009-918X


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  4 in total

Review 1.  Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy.

Authors:  Emanuela Viggiano; Manuela Ergoli; Esther Picillo; Luisa Politano
Journal:  Hum Genet       Date:  2016-04-21       Impact factor: 4.132

2.  Muscular dystrophy in girls with X;autosome translocations.

Authors:  Y Boyd; V Buckle; S Holt; E Munro; D Hunter; I Craig
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

3.  Mapping of X chromosome translocation breakpoints in females with Duchenne muscular dystrophy with respect to exons of the dystrophin gene.

Authors:  D J Cockburn; E A Munro; I W Craig; Y Boyd
Journal:  Hum Genet       Date:  1992-12       Impact factor: 4.132

4.  De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy.

Authors:  J Chelly; F Marlhens; B Le Marec; M Jeanpierre; M Lambert; G Hamard; B Dutrillaux; J C Kaplan
Journal:  Hum Genet       Date:  1986-10       Impact factor: 4.132
  4 in total

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