Literature DB >> 1572654

Genetic mapping on the mouse X chromosome of human cDNA clones for the fragile X and Hunter syndromes.

C J Faust1, A J Verkerk, P J Wilson, C P Morris, J J Hopwood, B A Oostra, G E Herman.   

Abstract

Murine X-linked genes corresponding to the human Fragile X (FMR1) and Hunter syndrome (IDS) loci have been mapped in an interspecific backcross between B6CBA-Aw-J/A-Bpa and Mus spretus using human cDNA clones. Pedigree analysis of recombinants from a total of 248 backcross progeny favors a gene order of (Cf-9, Mcf-2)-(Fmr-1)-Ids-Gabra3-Rsvp. Gene order is conserved between the species, although no fragile site has been detected in the mouse in this region of the murine X chromosome.

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Year:  1992        PMID： 1572654     DOI： 10.1016/0888-7543(92)90314-i

Source DB:  PubMed          Journal:  Genomics        ISSN： 0888-7543            Impact factor:   5.736


  4 in total

Review 1.  Mouse X chromosome.

Authors:  S D Brown; P Avner; G E Herman
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28.

Authors:  T A Angel; C J Faust; J C Gonzales; S Kenwrick; R A Lewis; G E Herman
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

3.  Comparative mapping on the mouse X chromosome defines a myotubular myopathy equivalent region.

Authors:  B de Gouyon; A Chatterjee; A Monaco; N Quaderi; S D Brown; G E Herman
Journal:  Mamm Genome       Date:  1996-08       Impact factor: 2.957

4.  Heterogeneity of DNA and RNA in Hunter patients.

Authors:  T Annella; A Daniele; P Di Natale
Journal:  Hum Genet       Date:  1993-10       Impact factor: 4.132
  4 in total

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