Literature DB >> 3016656

A TaqI RFLP in Xq26-Xqter detected by pX45h [HGM8 no. DXS100h].

K Wrogemann, B Arveiler, I Oberle, L M Mulligan, J A Holden, C J Forster-Gibson, B N White.   

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Year:  1986        PMID： 3016656      PMCID： PMC311570          DOI： 10.1093/nar/14.13.5572

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


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  1 in total

1.  Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.

Authors:  L M Mulligan; M A Phillips; C J Forster-Gibson; J Beckett; M W Partington; N E Simpson; J J Holden; B N White
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025
  1 in total
  2 in total

1.  Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.

Authors:  C Schwartz; N Fitch; M C Phelan; C L Richer; R Stevenson
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

2.  Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.

Authors:  I Oberlé; G Camerino; K Wrogemann; B Arveiler; A Hanauer; E Raimondi; J L Mandel
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132
  2 in total

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