Literature DB >> 8358436

A high resolution deletion map of human chromosome Xp22.

L Schaefer1, G B Ferrero, A Grillo, M T Bassi, E J Roth, M C Wapenaar, G J van Ommen, T K Mohandas, M Rocchi, H Y Zoghbi, A Ballabio.   

Abstract

We have developed a 32-interval deletion panel for human chromosome Xp22 spanning about 30 megabases of genomic DNA. DNA samples from 50 patients with chromosomal rearrangements involving Xp22 were tested with 60 markers using a polymerase chain reaction strategy. The ensuing deletion map allowed us to confirm and refine the order of previously isolated and newly developed markers. Our mapping panel will provide the framework for mapping new sequences, for orienting chromosome walks in the region and for projects aimed at isolating genes responsible for diseases mapping to Xp22.

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Year:  1993        PMID： 8358436     DOI： 10.1038/ng0793-272

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


  14 in total

1.  The Turner syndrome-associated neurocognitive phenotype maps to distal Xp.

Authors:  J L Ross; D Roeltgen; H Kushner; F Wei; A R Zinn
Journal:  Am J Hum Genet       Date:  2000-08-08       Impact factor: 11.025

Review 2.  SHOX gene in Leri-Weill syndrome and in idiopathic short stature.

Authors:  S Bernasconi; S Mariani; C Falcinelli; S Milioli; L Iughetti; A Forabosco
Journal:  J Endocrinol Invest       Date:  2001-10       Impact factor: 4.256

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.  Improved genetic mapping of X linked retinoschisis.

Authors:  N D George; S J Payne; R M Bill; D E Barton; A T Moore; J R Yates
Journal:  J Med Genet       Date:  1996-11       Impact factor: 6.318

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.  Pigmentation, pleiotropy, and genetic pathways in humans and mice.

Authors:  G S Barsh
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

7.  A de novo satellited short arm of the Y chromosome possibly resulting from an unstable translocation.

Authors:  C L Lin; L Gibson; B Pober; T L Yang-Feng
Journal:  Hum Genet       Date:  1995-11       Impact factor: 4.132

8.  Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.

Authors:  A R Zinn; V S Tonk; Z Chen; W L Flejter; H A Gardner; R Guerra; H Kushner; S Schwartz; V P Sybert; D L Van Dyke; J L Ross
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025

9.  Refinement of the localisation of the X linked keratosis follicularis spinulosa decalvans (KFSD) gene in Xp22.13-p22.2.

Authors:  J C Oosterwijk; M J van der Wielen; E van de Vosse; E Voorhoeve; E Bakker
Journal:  J Med Genet       Date:  1995-09       Impact factor: 6.318

10.  Phenotypic variability in X-linked ocular albinism: relationship to linkage genotypes.

Authors:  R E Schnur; P A Wick; C Bailey; T Rebbeck; R G Weleber; J Wagstaff; A W Grix; R A Pagon; A Hockey; M J Edwards
Journal:  Am J Hum Genet       Date:  1994-09       Impact factor: 11.025
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