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Meiotic drive at the myotonic dystrophy and the cone-rod dystrophy loci on chromosome 19q13.3.

作者信息

Inglehearn C F, Gregory C Y

出版信息

Am J Hum Genet. 1997 Jun;60(6):1562-3. doi: 10.1016/S0002-9297(07)64255-4.

Abstract
摘要

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引用本文的文献

本文引用的文献

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Abnormal Segregation in Hereditary Renal Disease with Deafness.
Am J Hum Genet. 1961 Mar;13(1 Pt 1):89-97.
2
Congenital Aniridia.
Am J Hum Genet. 1960 Dec;12(4 Pt 1):389-415.
3
Ectrodactyly--evidence in favour of a disturbed segregation in the offspring of affected males.
Ann Hum Genet. 1960 Apr;24:89-96. doi: 10.1111/j.1469-1809.1959.tb01719.x.
5
A 30-Mb metric fluorescence in situ hybridization map of human chromosome 19q.
Genomics. 1995 Nov 20;30(2):187-94. doi: 10.1006/geno.1995.9886.
6
Origin of the expansion mutation in myotonic dystrophy.
Nat Genet. 1993 May;4(1):72-6. doi: 10.1038/ng0593-72.
8
Meiotic drive at the myotonic dystrophy locus?
Nat Genet. 1994 Feb;6(2):117-8. doi: 10.1038/ng0294-117.
9
Meiotic drive at the myotonic dystrophy locus.
J Med Genet. 1994 Dec;31(12):980. doi: 10.1136/jmg.31.12.980.

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