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Linkage analysis of the Rett syndrome using human chromosomal specific probes

  • Published:1985-01 Issue:3 Volume:7 Page:361-364
  • ISSN:0387-7604
  • Container-title:Brain and Development
  • language:en
  • Short-container-title:Brain and Development

Author:

Anvret Maria,Johansson Ing-Marie,Wahlström Jan,Hagberg Bengt

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference17 articles.

1. Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation;Kan;Proc Natl Acad SCi USA,1978

2. Construction of a genetic linkage map in man using restriction fragment length polymorphisms;Botstern;Am J Hum Genet,1980

3. Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome;Davies;Nucl AcidRes,1983

4. Genetic mapping of the human X chromsome by using restriction fragment length polymorphisms;Drayna;Proc Natl Acad Sci USA,1984

5. DNA-analysis and the antenatal diagnosis of hemoglobinopathies;Little,1981

Cited by 15 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Japanese monozygotic twins with Rett syndrome;Brain and Development;1997-12

2. General discussion;Acta Paediatrica;1990-07

3. Brief report: Two sisters with Rett syndrome;Journal of Autism and Developmental Disorders;1990-03

4. Molecular analysis of the Rett syndrome using cDNA synapsin I as a probe;Brain and Development;1990-01

5. Rett Syndrome:;Physical & Occupational Therapy In Pediatrics;1989-01
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