Literature DB >> 3482420

Physical mapping studies on the human X chromosome in the region Xq27-Xqter.

M Patterson1, C Schwartz, M Bell, S Sauer, M Hofker, B Trask, G van den Engh, K E Davies.   

Abstract

We have characterized three terminal deletions of the long arm of the X chromosome. Southern analysis using Xq27/q28 probes suggests that two of the deletions have breakpoints near the fragile site at Xq27.3. Flow karyotype analysis provides an estimate of 12 X 10(6) bp for the size of the deleted region. We have not detected the deletion breakpoints by pulsed-field gel electrophoresis (PFGE) using the closet DNA probes, proximal to the fragile site. The physical distance between the breakpoints and the probes may therefore be several hundred kilobases. The use of the deletion patients has allowed a preliminary physical map of Xq27/28 to be constructed. Our data suggest that the closest probes to the fragile site on the proximal side are 4D-8 (DXS98), cX55.7 (DXS105), and cX33.2 (DXS152). PFGE studies provide evidence for the physical linkage of 4D-8, cX55.7, and cX33.2. We have also found evidence for the physical linkage of F8C, G6PD, and 767 (DXS115), distal to the fragile site.

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Year:  1987        PMID: 3482420     DOI: 10.1016/0888-7543(87)90028-0

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


  31 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  Inheritance of chromosome heteromorphisms analyzed by high-resolution bivariate flow karyotyping.

Authors:  B Trask; G van den Engh; J W Gray
Journal:  Am J Hum Genet       Date:  1989-11       Impact factor: 11.025

3.  Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locus.

Authors:  P Jedlicka; S Greer; D S Millar; C B Grundy; E Jenkins; M Mitchell; R S Mibashan; V V Kakkar; D N Cooper
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132

Review 4.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

5.  Microdissection of the fragile X region.

Authors:  R N MacKinnon; M C Hirst; M V Bell; J E Watson; U Claussen; H J Ludecke; G Senger; B Horsthemke; K E Davies
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

6.  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

Review 7.  The fragile X: progress toward solving the puzzle.

Authors:  W T Brown
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

8.  Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.

Authors:  C E Schwartz; J P Johnson; B Holycross; T M Mandeville; T S Sears; E A Graul; J C Carey; R J Schroer; M C Phelan; J Szollar
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

9.  Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28.

Authors:  M V Bell; J Bloomfield; M McKinley; M N Patterson; M G Darlison; E A Barnard; K E Davies
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

10.  A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome.

Authors:  A Vincent; C Kretz; I Oberlé; J L Mandel
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

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