Literature DB >> 1897527

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

A Henke1, M Wapenaar, G J van Ommen, P Maraschio, G Camerino, G Rappold.   

Abstract

Short stature is consistently found in individuals with terminal deletions of Xp. In order to refine the localization of a putative locus affecting height, we analyzed two patients with a partial monosomy of the pseudoautosomal region at the molecular level. Eight pseudoautosomal probes were used for the genetic deletion analysis through dose evaluation. Three of them represent new markers (DXS415, DXS419, and DXS406) which were positioned on the pseudoautosomal map by pulsed field gel electrophoresis. Our data suggest that a locus affecting height maps in a region of about 1.5 Mbp, distal to the DXS406 locus and proximal to the DXS415 locus, a region which includes two CpG islands, and rule out an involvement of very distal sequences at the X/Y telomeres.

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Year:  1991        PMID: 1897527      PMCID: PMC1683157     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  27 in total

Review 1.  KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS.

Authors:  M A FERGUSON-SMITH
Journal:  J Med Genet       Date:  1965-06       Impact factor: 6.318

2.  Two families of low-copy-number repeats are interspersed on Xp22.3: implications for the high frequency of deletions in this region.

Authors:  A Ballabio; B Bardoni; S Guioli; E Basler; G Camerino
Journal:  Genomics       Date:  1990-10       Impact factor: 5.736

3.  Isolation and characterization of cell hybrids containing human Xp-chromosome fragments.

Authors:  M C Wapenaar; T Kievits; P Meera Khan; P L Pearson; G J Van Ommen
Journal:  Cytogenet Cell Genet       Date:  1990

4.  Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome.

Authors:  E M Fisher; P Beer-Romero; L G Brown; A Ridley; J A McNeil; J B Lawrence; H F Willard; F R Bieber; D C Page
Journal:  Cell       Date:  1990-12-21       Impact factor: 41.582

Review 5.  CpG-rich islands and the function of DNA methylation.

Authors:  A P Bird
Journal:  Nature       Date:  1986 May 15-21       Impact factor: 49.962

6.  A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion.

Authors:  B G Herrmann; D P Barlow; H Lehrach
Journal:  Cell       Date:  1987-03-13       Impact factor: 41.582

7.  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

8.  The sex-determining region of the human Y chromosome encodes a finger protein.

Authors:  D C Page; R Mosher; E M Simpson; E M Fisher; G Mardon; J Pollack; B McGillivray; A de la Chapelle; L G Brown
Journal:  Cell       Date:  1987-12-24       Impact factor: 41.582

9.  Physical mapping of the human pseudo-autosomal region; comparison with genetic linkage map.

Authors:  C Petit; J Levilliers; J Weissenbach
Journal:  EMBO J       Date:  1988-08       Impact factor: 11.598

10.  A physical map of the human pseudoautosomal region.

Authors:  W R Brown
Journal:  EMBO J       Date:  1988-08       Impact factor: 11.598

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  6 in total

Review 1.  The pseudoautosomal regions of the human sex chromosomes.

Authors:  G A Rappold
Journal:  Hum Genet       Date:  1993-10       Impact factor: 4.132

2.  Ullrich-Turner syndrome is not caused by haploinsufficiency of RPS4X.

Authors:  C Geerkens; W Just; K R Held; W Vogel
Journal:  Hum Genet       Date:  1996-01       Impact factor: 4.132

3.  Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height.

Authors:  T Ogata; N Matsuo
Journal:  Hum Genet       Date:  1993-07       Impact factor: 4.132

4.  An analysis of Xq deletions.

Authors:  P Maraschio; R Tupler; L Barbierato; E Dainotti; D Larizza; F Bernardi; H Hoeller; A Garau; L Tiepolo
Journal:  Hum Genet       Date:  1996-03       Impact factor: 4.132

5.  Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation.

Authors:  M Joseph; E S Cantú; G S Pai; S M Willi; P R Papenhausen; L Weiss
Journal:  J Med Genet       Date:  1996-11       Impact factor: 6.318

6.  Chromosomal localisation of a pseudoautosomal growth gene(s).

Authors:  T Ogata; C Petit; G Rappold; N Matsuo; T Matsumoto; P Goodfellow
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

  6 in total

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