Literature DB >> 1685139

Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome.

R G Lafrenière1, C J Brown, V E Powers, L Carrel, K E Davies, D F Barker, H F Willard.   

Abstract

Using a panel of human/rodent somatic cell hybrids and human lymphoblast lines segregating 18 different human X-chromosome rearrangements and deletions, we have assigned 60 DNA markers to the physical map of the X chromosome from Xp21.1 to Xq21.3. Data from Southern blot hybridization and polymerase chain reaction (PCR) amplification assign these markers to 15 primary map intervals. This provides a basis for further long-range cloning and mapping of the pericentromeric region of the X chromosome.

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Year:  1991        PMID: 1685139     DOI: 10.1016/0888-7543(91)90143-3

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  21 in total

1.  PCR amplification of tandemly repeated DNA: analysis of intra- and interchromosomal sequence variation and homologous unequal crossing-over in human alpha satellite DNA.

Authors:  P E Warburton; H F Willard
Journal:  Nucleic Acids Res       Date:  1992-11-25       Impact factor: 16.971

2.  Dinucleotide repeat polymorphism at the DXS441 locus.

Authors:  K T Ram; D F Barker; J M Puck
Journal:  Nucleic Acids Res       Date:  1992-03-25       Impact factor: 16.971

Review 3.  Genetic deficiencies of the glycogen phosphorylase system.

Authors:  J Hendrickx; P J Willems
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

Review 4.  Regulation of X-chromosome inactivation by the X-inactivation centre.

Authors:  Sandrine Augui; Elphège P Nora; Edith Heard
Journal:  Nat Rev Genet       Date:  2011-06       Impact factor: 53.242

5.  Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis.

Authors:  T Lester; M de Alwis; P A Clark; A M Jones; F Katz; R J Levinsky; C Kinnon
Journal:  J Med Genet       Date:  1994-09       Impact factor: 6.318

6.  Refinement of the X-linked cleft palate and ankyloglossia (CPX) localisation by genetic mapping in an Icelandic kindred.

Authors:  S A Forbes; M Richardson; L Brennan; A Arnason; A Bjornsson; L Campbell; G Moore; P Stanier
Journal:  Hum Genet       Date:  1995-03       Impact factor: 4.132

7.  Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpoints.

Authors:  R J Sinke; B de Leeuw; H A Janssen; D O Weghuis; R F Suijkerbuijk; A M Meloni; S Gilgenkrantz; W Berger; H H Ropers; A A Sandberg
Journal:  Hum Genet       Date:  1993-10-01       Impact factor: 4.132

8.  High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus.

Authors:  J Zonana; M Jones; D Browne; M Litt; P Kramer; H W Becker; N Brockdorff; S Rastan; K P Davies; A Clarke
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

9.  Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family.

Authors:  F A Hol; M P Geurds; O Jensson; B C Hamel; G E Moore; R Newton; E C Mariman
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

10.  Partial inversion of gene order within a homologous segment on the X chromosome.

Authors:  S H Laval; Y Boyd
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

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