Literature DB >> 3674754

Physical mapping of genes and sequences at the end of the human X chromosome short arm.

C Mondello1, H H Ropers, I W Craig, E Tolley, P N Goodfellow.   

Abstract

Human-rodent somatic cell hybrids containing deleted and translocated human X chromosomes have been used to map genes and sequences in and around the pseudoautosomal region. The following order was found: (DXS69, DXS70, DXS143)-(DXS31, STS)-MIC2. This order is consistent with the known inheritance patterns of DXS31, STS and MIC2. Assuming that the translocations and deletions we have studied are not complex rearrangements, we conclude that the pseudoautosomal region consists of less than 5 X 10(6) bp of DNA.

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Year:  1987        PMID： 3674754     DOI： 10.1111/j.1469-1809.1987.tb01055.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN： 0003-4800            Impact factor:   1.670


  9 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  Short stature in a girl with a terminal Xp deletion distal to DXYS15: localisation of a growth gene(s) in the pseudoautosomal region.

Authors:  T Ogata; P Goodfellow; C Petit; M Aya; N Matsuo
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

Review 3.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

4.  Deletions within the pseudoautosomal region help map three new markers and indicate a possible role of this region in linear growth.

Authors:  A Henke; M Wapenaar; G J van Ommen; P Maraschio; G Camerino; G Rappold
Journal:  Am J Hum Genet       Date:  1991-10       Impact factor: 11.025

5.  Long-range restriction map of the terminal part of the short arm of the human X chromosome.

Authors:  C Petit; J Levilliers; J Weissenbach
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

6.  An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome.

Authors:  R G Knowlton; C A Nelson; V A Brown; D C Page; H Donis-Keller
Journal:  Nucleic Acids Res       Date:  1989-01-11       Impact factor: 16.971

7.  A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval.

Authors:  A Klink; A Meindl; H Hellebrand; G A Rappold
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

8.  Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.

Authors:  A Ballabio; B Bardoni; R Carrozzo; G Andria; D Bick; L Campbell; B Hamel; M A Ferguson-Smith; G Gimelli; M Fraccaro
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

9.  A long range restriction map of the pseudoautosomal region by partial digest PFGE analysis from the telomere.

Authors:  G A Rappold; H Lehrach
Journal:  Nucleic Acids Res       Date:  1988-06-24       Impact factor: 16.971
  9 in total

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