Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndrome-Reference-Cited by-同舟云学术

Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndrome

Published:1984-03 Issue:1 Volume:66 Page:54-56
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Davies K. E.,Harper K.,Bonthron D.,Krumlauf R.,Polkey A.,Pembrey M. E.,Williamson R.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00275186.pdf

Reference9 articles.

1. Davies KE (1981) The application of DNA recombinant technology to the analysis of the human genome and genetic disease. Hum Genet 58:351?357

2. Davies KE (1983) Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome. Nucleic Acids Res 8: 2303?2312

3. Hamerton JL (1982) Population cytogenetics: a perspective. In: Adinolfi M (ed) Paediatric research?A genetic approach. Heinemann, London, pp 99?121

4. Krumlauf R, Jeanpierre M, Young BD (1982) Construction and characterisation of genomic libraries from specific human chromosomes. Proc Natl Acad Sci USA 79:2971?2975

5. Kunkel LM, Smith KD, Boyer SH, Borgaonkar DS, Wachtel sS, Miller OJ, Breg WR, Jones HW, Rary JM (1977) Analysis of human Y-chromosome specific reiterated DNA in chromosome variants. Proc Natl Acad Sci USA 74:1245?1249

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