Investigation of a Family with Autosomal Dominant Dilated Cardiomyopathy Defines a Novel Locus on Chromosome 2q14-q22
- 1 October 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (4), 1068-1077
- https://doi.org/10.1086/302580
Abstract
No abstract availableKeywords
This publication has 41 references indexed in Scilit:
- Guidelines for the study of familial dilated cardiomyopathiesEuropean Heart Journal, 1999
- Linkage of Familial Dilated Cardiomyopathy with Conduction Defect and Muscular Dystrophy to Chromosome 6q23American Journal of Human Genetics, 1997
- Mapping a cardiomyopathy locus to chromosome 3p22-p25.JCI Insight, 1996
- A Point Mutation in the 5' Splice Site of the Dystrophin Gene First Intron Responsible for X-Linked Dilated CardiomyopathyHuman Molecular Genetics, 1996
- The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set–recoding and fuzzy inheritanceNature Genetics, 1995
- A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysisNeuromuscular Disorders, 1995
- LODVIEW: A Computer Program for the Graphical Evaluation of Lod Score Results in Exclusion Mapping of Human Disease GenesComputers and Biomedical Research, 1993
- X-Linked Dilated CardiomyopathyNew England Journal of Medicine, 1987
- Echocardiographic measurements in normal subjects from infancy to old age.Circulation, 1980
- The use of single plane angiocardiograms for the calculation of left ventricular volume in manAmerican Heart Journal, 1968