Literature DB >> 7759082

Refinement of the locus for X-linked recessive chondrodysplasia punctata.

K Muroya1, T Ogata, G Rappold, A Klink, Y Nakahori, Y Fukushima, K Aizu, N Matsuo.   

Abstract

Although the locus for X-linked recessive chondrodysplasia punctata (CDPX1) has been mapped to the region between PABX and DXS31 (the critical region is about 3 Mb long), the precise location within the critical region has not been determined. In this paper, we describe a boy with a 46,Y,der(X)t(X;Y)(p22.3;q11)mat karyotype and review the genotype-phenotype correlations in three male patients with the combination of apparent lack of clinical features of CDPX1 and a partial deletion of the critical region. The results suggest that the region defined by the two BssHII sites at 3180 and 3570 kb from the Xp telomere may be the target region for the CDPX1 locus.

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Year:  1995        PMID: 7759082     DOI: 10.1007/BF00223874

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  14 in total

1.  An RFLP detecting single copy X-chromosome fragment, dic56, from Xp22-Xpter [HGM8 assignment no. DXS 143].

Authors:  W Middlesworth; C Bertelson; L M Kunkel
Journal:  Nucleic Acids Res       Date:  1985-08-12       Impact factor: 16.971

2.  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

3.  Long-range physical mapping around the human steroid sulfatase locus.

Authors:  M T Ross; A Ballabio; I W Craig
Journal:  Genomics       Date:  1990-03       Impact factor: 5.736

4.  Radiographic measurements of metacarpophalangeal lengths in Japanese children.

Authors:  S Matsuura; T Kajii
Journal:  Jinrui Idengaku Zasshi       Date:  1989-06

5.  Absent chondrodysplasia punctata in a male with an Xp terminal deletion involving the putative region for CDPX1 locus.

Authors:  T Ogata; P Goodfellow; C Petit; P Maroteaux; N Matsuo
Journal:  Am J Med Genet       Date:  1993-01-01

6.  A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata.

Authors:  D Weil; M F Portnoï; J Levilliers; I Wang; M Mathieu; J L Taillemite; M Meier; B Boudailliez; C Petit
Journal:  Hum Mol Genet       Date:  1993-11       Impact factor: 6.150

7.  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

8.  Brachytelephalangic chondrodysplasia punctata: a possible X-linked recessive form.

Authors:  P Maroteaux
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

9.  A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.

Authors:  M Koenig; G Camerino; R Heilig; J L Mandel
Journal:  Nucleic Acids Res       Date:  1984-05-25       Impact factor: 16.971

10.  An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature.

Authors:  C Petit; J Melki; J Levilliers; F Serville; J Weissenbach; P Maroteaux
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

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  2 in total

1.  FISH deletion mapping defines a single location for the Y chromosome stature gene, GCY.

Authors:  S Kirsch; B Weiss; M De Rosa; T Ogata; G Lombardi; G A Rappold
Journal:  J Med Genet       Date:  2000-08       Impact factor: 6.318

2.  Brachytelephalangic chondrodysplasia punctata with severe spinal cord compression: report of four new cases.

Authors:  Arnaud Garnier; Stéphane Dauger; Danièle Eurin; Ida Parisi; Giancarlo Parenti; Catherine Garel; Katy Delbecque; Clarisse Baumann
Journal:  Eur J Pediatr       Date:  2006-08-26       Impact factor: 3.183

  2 in total

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