Mapping of a first locus for autosomal dominant myxomatous mitral-valve prolapse to chromosome 16p11.2-p12.1.
about
Human polyserase-2, a novel enzyme with three tandem serine protease domains in a single polypeptide chainMitral valve disease--morphology and mechanisms.Epidemiology and pathophysiology of mitral valve prolapse: new insights into disease progression, genetics, and molecular basisDifferentiating the aging of the mitral valve from human and canine myxomatous degenerationGenetics of valvular heart diseaseDegenerative mitral valve disease with emphasis on mitral valve prolapseIdentification and characterization of human polyserase-3, a novel protein with tandem serine-protease domains in the same polypeptide chain.A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.Expression of the familial cardiac valvular dystrophy gene, filamin-A, during heart morphogenesis.Toward an understanding of the cause of mitral valve prolapseGenetic aspects of arrhythmias.Mild expression of mitral valve prolapse in the Framingham offspring: expanding the phenotypic spectrum.Basic mechanisms of mitral regurgitation.Further genetic evidence for a panic disorder syndrome mapping to chromosome 13q.Familial clustering of mitral valve prolapse in the community.Targeted Mybpc3 Knock-Out Mice with Cardiac Hypertrophy Exhibit Structural Mitral Valve AbnormalitiesAutonomic dysregulation as a novel underlying cause of mitral valve prolapse: a hypothesisGenetic association analyses highlight biological pathways underlying mitral valve prolapse.Differential MicroRNA Expression Profile in Myxomatous Mitral Valve Prolapse and Fibroelastic Deficiency ValvesMarfan syndrome and mitral valve prolapse.Heart valve structure and function in development and diseaseDegenerative mitral valve regurgitation: understanding basic concepts and new developments.Filamin-a-related myxomatous mitral valve dystrophy: genetic, echocardiographic and functional aspects.Mitral valve disease in Marfan syndrome and related disorders.Current Discoveries and Interventions for Barlow's Disease.Mitral valve prolapse: a deeper look.Mitral Valve Prolapse: Multimodality Imaging and Genetic Insights.Genetics of syndromic and non-syndromic mitral valve prolapse.Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse.Genomic analysis in patients with myxomatous mitral valve prolapse: current state of knowledge.Familial cardiac valvulopathy due to filamin A mutation.Screening of TGFBR1, TGFBR2, and FLNA in familial mitral valve prolapse.Fibrillin-1 gene intron 56 polymorphism in Turkish children with mitral valve prolapse.Infektiöse EndokarditisGENETIC FIBRILLINOPATHIES : NEW INSIGHTS IN MOLECULAR DIAGNOSIS AND CLINICAL MANAGEMENT
P2860
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P2860
Mapping of a first locus for autosomal dominant myxomatous mitral-valve prolapse to chromosome 16p11.2-p12.1.
description
1999 nî lūn-bûn
@nan
1999 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Mapping of a first locus for a ...... e to chromosome 16p11.2-p12.1.
@ast
Mapping of a first locus for a ...... e to chromosome 16p11.2-p12.1.
@en
Mapping of a first locus for a ...... e to chromosome 16p11.2-p12.1.
@nl
type
label
Mapping of a first locus for a ...... e to chromosome 16p11.2-p12.1.
@ast
Mapping of a first locus for a ...... e to chromosome 16p11.2-p12.1.
@en
Mapping of a first locus for a ...... e to chromosome 16p11.2-p12.1.
@nl
prefLabel
Mapping of a first locus for a ...... e to chromosome 16p11.2-p12.1.
@ast
Mapping of a first locus for a ...... e to chromosome 16p11.2-p12.1.
@en
Mapping of a first locus for a ...... e to chromosome 16p11.2-p12.1.
@nl
P2093
P2860
P356
P1476
Mapping of a first locus for a ...... e to chromosome 16p11.2-p12.1.
@en
P2093
Carpentier A
Le Heuzey JY
P2860
P304
P356
10.1086/302624
P407
P577
1999-11-01T00:00:00Z