Construction of a PAC contig of the 1.5 Mb CMT1A duplication HNPP deletion region in 17p11.2-p12 for the purpose of a large scale sequencing effort.

被引：0
|
作者：
Inoue, K [1 ]
Murakami, T [1 ]
Reiter, LT [1 ]
Koeuth, T [1 ]
Chinault, C [1 ]
Lupski, JR [1 ]
机构：
[1] Baylor Coll Med, Houston, TX 77030 USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1997年 / 61卷 / 04期
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中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
1367
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页码：A235 / A235
页数：1
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    Kabzinska, D.
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