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Literature DB >> 6684694

The fragile X: a scanning electron microscope study.

C J Harrison, E M Jack, T D Allen, R Harris.

Abstract

Scanning electron microscopy (SEM) has been used to study the fragile X chromosome. The fragile site appears as an isochromatid gap in the majority of cases, confirming light microscope (LM) observations. SEM has allowed a more precise location of the fragile site to the Xq27 . 3 region.

Entities: Disease

Mesh：

Year: 1983 PMID： 6684694 PMCID： PMC1049120 DOI： 10.1136/jmg.20.4.280

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

9 in total

1. High resolution of human chromosomes.

Authors: J J Yunis
Journal: Science Date: 1976-03-26 Impact factor: 47.728

2. Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture.

Authors: G R Sutherland
Journal: Am J Hum Genet Date: 1979-03 Impact factor: 11.025

3. Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics.

Authors: G R Sutherland
Journal: Am J Hum Genet Date: 1979-03 Impact factor: 11.025

4. A rapid banding technique for human chromosomes.

Authors: M Seabright
Journal: Lancet Date: 1971-10-30 Impact factor: 79.321

5. Scanning electron microscopy of the G-banded human karyotype.

Authors: C J Harrison; M Britch; T D Allen; R Harris
Journal: Exp Cell Res Date: 1981-07 Impact factor: 3.905

6. Metaphase chromosome structure: evidence for a radial loop model.

Authors: M P Marsden; U K Laemmli
Journal: Cell Date: 1979-08 Impact factor: 41.582

7. The characterization of high-resolution G-banded chromosomes of man.

Authors: J J Yunis; J R Sawyer; D W Ball
Journal: Chromosoma Date: 1978-08-14 Impact factor: 4.316

8. High resolution scanning electron microscopy of isolated and in situ cytoskeletal elements.

Authors: W Ip; D A Fischman
Journal: J Cell Biol Date: 1979-10 Impact factor: 10.539

9. High-resolution scanning electron microscopy of human metaphase chromosomes.

Authors: C J Harrison; T D Allen; M Britch; R Harris
Journal: J Cell Sci Date: 1982-08 Impact factor: 5.285

9 in total

22 in total

1. Visualization by atomic force microscopy and FISH of the 45S rDNA gaps in mitotic chromosomes of Lolium perenne.

Authors: Jing Huang; Lu Ma; Sriram Sundararajan; Shui-zhang Fei; Lijia Li
Journal: Protoplasma Date: 2009-05-26 Impact factor: 3.356

2. Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locus.

Authors: R Sood; L M Mulligan; R Poon; B N White; J J Holden
Journal: Am J Hum Genet Date: 1990-09 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. In situ hybridization studies using a molecular probe that maps to Xq27-Zq28.

Authors: A M Duncan; C Morgan
Journal: Hum Genet Date: 1990-04 Impact factor: 4.132

5. Fragile X syndrome: clinical, cytogenetic, biochemical and molecular features.

Authors: J C Mixon; V G Dev
Journal: Indian J Pediatr Date: 1986 Jul-Aug Impact factor: 1.967

6. The fragile site (16)(q22). II. Sister chromatid exchanges.

Authors: M Schmid; W Feichtinger; T Haaf
Journal: Hum Genet Date: 1987-08 Impact factor: 4.132

7. Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.

Authors: J M Connor; L A Pirrit; J R Yates; J A Crossley; S J Imrie; J M Colgan
Journal: J Med Genet Date: 1987-01 Impact factor: 6.318