Literature DB >> 3460742

Regional localization of 18 human X-linked DNA sequences.

D C Riddell, H S Wang, J Beckett, A Chan, J J Holden, L M Mulligan, M A Phillips, N E Simpson, K Wrogemann, J L Hamerton.   

Abstract

A series of human probes with unique sequences has been isolated from a recombinant phage library constructed with DNA obtained from a human-hamster hybrid cell line. This cell line contained the X chromosome as the only human component. For 18 of these probes, a human X-chromosome origin has been confirmed and they have been regionally assigned by a combination of techniques: dosage studies utilizing DNA from human fibroblasts carrying X-chromosome duplications and deletions; the presence or absence of hybridization to digested DNA from hybrid lines carrying fragments of the X chromosome; and in situ hybridization to metaphase chromosomes. The use of dosage as a means to regionally assign probes significantly improves resolution of the X chromosome.

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Year:  1986        PMID: 3460742     DOI: 10.1159/000132264

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  13 in total

1.  Physical mapping of an Xq-proximal interstitial duplication in a male.

Authors:  F Muscatelli; J M Verna; N Philip; A Moncla; M G Mattei; J F Mattei; M Fontes
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

2.  Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.

Authors:  M Schmidt; A Certoma; D Du Sart; P Kalitsis; M Leversha; K Fowler; L Sheffield; I Jack; D M Danks
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

3.  Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X.

Authors:  V J Hyland; K E Fernandez; D F Callen; R N MacKinnon; E Baker; K Friend; G R Sutherland
Journal:  Hum Genet       Date:  1989-08       Impact factor: 4.132

4.  Isolation and mapping of a polymorphic DNA sequence, DXS312, to Xq27----Xq28.

Authors:  L Mulligan; R Sood; R Poon; B N White; J J Holden
Journal:  Nucleic Acids Res       Date:  1989-06-12       Impact factor: 16.971

5.  Characterization of chromatin at structurally abnormal inactive X chromosomes reveals potential evidence of a rare hybrid active and inactive isodicentric X chromosome.

Authors:  Brian P Chadwick
Journal:  Chromosome Res       Date:  2019-11-27       Impact factor: 5.239

6.  X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.

Authors:  J Zonana; A Clarke; M Sarfarazi; N S Thomas; K Roberts; K Marymee; P S Harper
Journal:  Am J Hum Genet       Date:  1988-07       Impact factor: 11.025

7.  A DNA marker closely linked to the factor IX (haemophilia B) gene.

Authors:  L Mulligan; J J Holden; B N White
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

8.  Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome.

Authors:  S Szpiro-Tapia; A Sefiani; M Guilloud-Bataille; S Heuertz; B Le Marec; J Frézal; P Maroteaux; M C Hors-Cayla
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

9.  DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.

Authors:  C R Greenberg; J L Hamerton; M Nigli; K Wrogemann
Journal:  Am J Hum Genet       Date:  1987-08       Impact factor: 11.025

10.  Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq.

Authors:  F P Cremers; T J van de Pol; B Wieringa; M H Hofker; P L Pearson; R A Pfeiffer; M Mikkelsen; A Tabor; H H Ropers
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

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