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Literature DB >> 2565864

Physical mapping of DXS134 close to the DXS52 locus.

M V Bell¹, M N Patterson, H R Dorkins, K E Davies.

Abstract

The locus DXS134 (cpX67) has been physically linked to the cluster of polymorphic loci DXS52, DXS15, and DXS33. A comparison of physical and genetic distance indicates a high rate of recombination in this region.

Mesh：

Year: 1989 PMID： 2565864 DOI： 10.1007/BF00288266

Source DB: PubMed Journal: Hum Genet ISSN： 0340-6717 Impact factor: 4.132

15 in total

1. The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.

Authors: I Oberlé; D Drayna; G Camerino; R White; J L Mandel
Journal: Proc Natl Acad Sci U S A Date: 1985-05 Impact factor: 11.205

2. Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3.

Authors: M Patterson; M Bell; C Schwartz; K Davies
Journal: Am J Med Genet Date: 1988 May-Jun

3. Resolution of DNA molecules greater than 5 megabases by contour-clamped homogeneous electric fields.

Authors: D Vollrath; R W Davis
Journal: Nucleic Acids Res Date: 1987-10-12 Impact factor: 16.971

4. Separation of large DNA molecules by contour-clamped homogeneous electric fields.

Authors: G Chu; D Vollrath; R W Davis
Journal: Science Date: 1986-12-19 Impact factor: 47.728

Review 5. Fragile X syndrome: a unique mutation in man.

Authors: R L Nussbaum; D H Ledbetter
Journal: Annu Rev Genet Date: 1986 Impact factor: 16.830

6. Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation.

Authors: M H Hofker; A A Bergen; M I Skraastad; N J Carpenter; H Veenema; J M Connor; E Bakker; G J van Ommen; P L Pearson
Journal: Am J Hum Genet Date: 1987-04 Impact factor: 11.025

7. Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.

Authors: D Drayna; K Davies; D Hartley; J L Mandel; G Camerino; R Williamson; R White
Journal: Proc Natl Acad Sci U S A Date: 1984-05 Impact factor: 11.205

8. The frequency of the fragile X chromosome among schoolchildren in Coventry.

Authors: T P Webb; S Bundey; A Thake; J Todd
Journal: J Med Genet Date: 1986-10 Impact factor: 6.318

9. The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.

Authors: H Veenema; N J Carpenter; E Bakker; M H Hofker; A M Ward; P L Pearson
Journal: J Med Genet Date: 1987-07 Impact factor: 6.318

10. Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.

Authors: G Camerino; M G Mattei; J F Mattei; M Jaye; J L Mandel
Journal: Nature Date: 1983 Dec 15-21 Impact factor: 49.962

5 in total

1. Further localization of X-linked hydrocephalus in the chromosomal region Xq28.

Authors: P J Willems; L Vits; P Raeymaekers; J Beuten; P Coucke; J J Holden; C Van Broeckhoven; S T Warren; M Sagi; D Robinson
Journal: Am J Hum Genet Date: 1992-08 Impact factor: 11.025

2. 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

Review 3. The fragile X: progress toward solving the puzzle.

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

4. Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome.

Authors: R Feil; G Palmieri; M d'Urso; R Heilig; I Oberlé; J L Mandel
Journal: Am J Hum Genet Date: 1990-04 Impact factor: 11.025

5. Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28.

Authors: P A Bolhuis; G W Hensels; T J Hulsebos; F Baas; P G Barth
Journal: Am J Hum Genet Date: 1991-03 Impact factor: 11.025

5 in total