Use of an autosomal dominant cataract (ADC) specific linkage panel to screen ADC pedigrees

被引：0

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作者：

Penrose, PJ

Johannes, M

Geyer, DD

Clancy, KP

Spence, MA

Bateman, JB

机构：

来源：

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 1999年 / 40卷 / 04期

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D O I：

暂无

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

4687B490

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页码：S889 / S889

页数：1

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[31] A COMPLETE SCREEN FOR MUTATIONS OF THE RHODOPSIN GENE IN A PANEL OF CHINESE PATIENTS WITH AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA
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[32] Sequence analyses of the lens intrinsic membrane protein 2 (LIM2, MP19) candidate gene in an autosomal dominant cataract family (ADC4).
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[33] GENETIC-LINKAGE OF AUTOSOMAL-DOMINANT JUVENILE GLAUCOMA TO 1Q21-Q31 IN 3 AFFECTED PEDIGREES
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[34] GENETIC-LINKAGE OF AUTOSOMAL-DOMINANT JUVENILE GLAUCOMA TO 1Q21-Q31 IN 3 AFFECTED PEDIGREES
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[35] The use of ultrasonography and linkage studies for early diagnosis of autosomal dominant polycystic kidney disease (ADPKD)
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[36] Linkage analysis in an autosomal dominant ‘zonular nuclear pulverulent’ congenital cataract, mapped to chromosome 13q11-13
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[37] Linkage analysis in an autosomal dominant 'zonular nuclear pulverulent' congenital cataract, mapped to chromosome 13q11-13
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[38] A new locus for autosomal dominant cataract on chromosome 19: Linkage analyses and screening of candidate genes (Vol 47, pg 3441, 2006)
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INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2006, 47 (09) : 4179 - 4180
[39] USE OF MOLECULAR HAPLOTYPES SPECIFIC FOR THE HUMAN PRO-ALPHA-2(I) COLLAGEN GENE IN LINKAGE ANALYSIS OF THE MILD AUTOSOMAL DOMINANT FORMS OF OSTEOGENESIS IMPERFECTA
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[40] Mapping of the human CP49 gene and identification of an intragenic polymorphic marker to allow genetic linkage analysis in autosomal dominant congenital cataract
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