Literature DB >> 8595402

An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3.

G B Ferrero1, B Franco, E J Roth, B A Firulli, G Borsani, J Delmas-Mata, J Weissenbach, G Halley, D Schlessinger, A C Chinault, H Y Zoghbi, D L Nelson, A Ballabio.   

Abstract

We have constructed a detailed physical map of the 35 Mb region spanning human chromosome Xp22.3-Xp21.3. The backbone of the map is represented by a single oriented contiguous stretch of 585 overlapping yeast artificial chromosome (YAC) clones covering the entire region. The map is formatted with 615 map objects that include 324 YACs, 185 sequence tagged sites, 28 genes, 85 chromosomal breakpoints and 37 highly polymorphic markers. Physical mapping was both guided and confirmed using 183 bins defined by chromosomal breakpoints and by overlapping regions of YAC clones. The localization of polymorphic markers in the physical map permits the integration of physical and genetic data across the region. These data establish chromosome Xp22.3-Xp21.3 as one of the best characterized large regions in the human genome. The map should greatly facilitate finer scale mapping and sequencing as well as the identification of disease genes from this portion of the human genome.

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Year:  1995        PMID: 8595402     DOI: 10.1093/hmg/4.10.1821

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  11 in total

1.  Deletion mapping and X inactivation analysis of a non-specific mental retardation gene at Xp21.3-Xp22.11.

Authors:  K Muroya; E Kinoshita; T Kamimaki; N Matsuo; T Yorifugi; T Ogata
Journal:  J Med Genet       Date:  1999-03       Impact factor: 6.318

2.  A gene spans the pseudoautosomal boundary in mice.

Authors:  S Palmer; J Perry; D Kipling; A Ashworth
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-28       Impact factor: 11.205

3.  Differential structuring of human populations for homologous X and Y microsatellite loci.

Authors:  R Scozzari; F Cruciani; P Malaspina; P Santolamazza; B M Ciminelli; A Torroni; D Modiano; D C Wallace; K K Kidd; A Olckers; P Moral; L Terrenato; N Akar; R Qamar; A Mansoor; S Q Mehdi; G Meloni; G Vona; D E Cole; W Cai; A Novelletto
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

4.  Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisis.

Authors:  L Huopaniemi; A Rantala; E Tahvanainen; A de la Chapelle; T Alitalo
Journal:  Am J Hum Genet       Date:  1997-05       Impact factor: 11.025

5.  High-resolution mapping by YAC fragmentation of a 2.5-Mb Xp22 region containing the human RS, KFSD and CLS disease genes.

Authors:  E Van de Vosse; P Van der Bent; J J Heus; G J Van Ommen; J T Den Dunnen
Journal:  Mamm Genome       Date:  1997-07       Impact factor: 2.957

6.  Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome.

Authors:  L M Brzustowicz; S Farrell; M B Khan; R Weksberg
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

7.  Evidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping.

Authors:  S Lien; J Szyda; B Schechinger; G Rappold; N Arnheim
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

8.  A novel syndrome of episodic muscle weakness maps to xp22.3.

Authors:  M M Ryan; P Taylor; J A Donald; R A Ouvrier; G Morgan; G Danta; M F Buckley; K N North
Journal:  Am J Hum Genet       Date:  1999-10       Impact factor: 11.025

9.  X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats.

Authors:  M T Bassi; R S Ramesar; B Caciotti; I M Winship; A De Grandi; M Riboni; P L Townes; P Beighton; A Ballabio; G Borsani
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

10.  A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation.

Authors:  M Fukami; S Kirsch; S Schiller; A Richter; V Benes; B Franco; K Muroya; E Rao; S Merker; B Niesler; A Ballabio; W Ansorge; T Ogata; G A Rappold
Journal:  Am J Hum Genet       Date:  2000-07-20       Impact factor: 11.025

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