

Author: Osoegawa K. Susukida R. Okano S. Kudoh J. Minoshima S. Shimizu N. de Jong P.J. Groet J. Ives J. Lehrach H. Nizetic D. Soeda E.
Publisher: Academic Press
ISSN: 0888-7543
Source: Genomics, Vol.32, Iss.3, 1996-03, pp. : 375-387
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Abstract
The major phenotypic features of Down syndrome have been correlated with partial trisomies of chromosome 21, allowing us to define the candidate gene region to a 4-Mb segment on the 21q22.2 band. We present here a high-resolution physical map with megabase-sized cosmid/PAC contigs. This ordered clone library has provided unique material for the integration of a variety of mappable objects, including exons, cDNAs, restriction sites, etc. Furthermore, our results have exemplified a strategy for the completion of the chromosome 21 map to sequencing.
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