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An ancestral core haplotype defines the critical region harbouring the North Carolina macular dystrophy gene (MCDR1)

Sauer, C G, Schworm, H D, Ulbig, M, Blankenagel, A, Rohrschneider, K, Pauleikhoff, D, Grimm, T and Weber, Bernhard H. F. (1997) An ancestral core haplotype defines the critical region harbouring the North Carolina macular dystrophy gene (MCDR1). Journal of Medical Genetics 34 (12), pp. 961-966.

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Abstract

Autosomal dominant North Carolina macular dystrophy (NCMD) or central areolar pigment epithelial dystrophy (CAPED) is an allelic disorder that maps to an approximately 7.2 cM interval between DNA markers at D6S424 and D6S1671 on 6q14-q16.2. The further refinement of the disease locus has been hindered by the lack of additional recombination events involving the critical region. In this study, we ...

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Item type:Article
Date:1997
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1136/jmg.34.12.961DOI
PMC1051143PubMedCentral-ID
9429134PubMed ID
Dewey Decimal Classification:600 Technology > 610 Medical sciences Medicine
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:No
Item ID:35338
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