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in Clin Genet

Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3

J. Kühnisch et al.
in J Am Heart Assoc

RIKADA study reveals risk factors in pediatric primary cardiomyopathy

N. Al-Wakeel-Marquard et al.
in Cell

The translational landscape of the human heart

S. van Heesch et al.
in J Am Coll Cardiol

Left ventricular noncompaction: phenotype in an integrated model of cardiomyopathy?

E. Oechslin et al.
in PLoS ONE

Loss of murine Gfi1 causes neutropenia and induces osteoporosis depending on the pathogen load and systemic inflammation

S. Geissler et al.
in Hum Mol Genet

The progressive ankyloses protein ANK facilitates clathrin- and adaptor-mediated membrane traffic at the trans-Golgi network-to-endosome interface

W. Seifert et al.
in Nat Genet

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

A. Sifrim et al.
in Dtsch Med Wochenschr

Position paper of cardiovascular disease : genetic diagnostics in cardiovascular diseases [Positionspapier Kardiovaskulaere Erkrankungen: Gendiagnostik bei kardiovaskulaeren Erkrankungen ]

E. Schulze-Bahr et al.
in Circ Cardiovasc Genet

Malformations of the left ventricle: what comes first: form or function?

S. Klaassen
in Kardiologe

Gendiagnostik bei kardiovaskulären Erkrankungen: Positionspapier der Deutschen Gesellschaft für Kardiologie (DGK) und der Deutschen Gesellschaft für Pädiatrische Kardiologie (DGPK) [Molecular diagnostics of cardiovascular diseases: Expert consensus st

E. Schulze-Bahr et al.