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Results: 1-12 |
Results: 12
IDENTIFICATION OF A NOVEL GENE FOR AUTOSOMAL-DOMINANT AND AUTOSOMAL RECESSIVE LONG-QT SYNDROME
Authors: SCHULZEBAHR,"WANG Q OBERTI C WEDEKIND H LANGE S BORGGREFE M TOWBIN JA ASSMANN G BREITHARDT G HAVERKAMP W FUNKE H
Citation: Q. Schulzebahr,"wang et al., IDENTIFICATION OF A NOVEL GENE FOR AUTOSOMAL-DOMINANT AND AUTOSOMAL RECESSIVE LONG-QT SYNDROME, European journal of human genetics, 6, 1998, pp. 4283-4283
KCNE1 MUTATIONS CAUSE JERVELL AND LANGE-NIELSEN-SYNDROME
Authors: SCHULZEBAHR E WANG Q WEDEKIND H HAVERKAMP W CHEN QY SUN YL RUBIE C HORDT M TOWBIN JA BORGGREFE M ASSMANN G QU XD SOMBERG JC BREITHARDT G OBERTI C FUNKE H
Citation: E. Schulzebahr et al., KCNE1 MUTATIONS CAUSE JERVELL AND LANGE-NIELSEN-SYNDROME, Nature genetics, 17(3), 1997, pp. 267-268
AUTOSOMAL RECESSIVE LONG-QT SYNDROME (JERVELL LANGE-NIELSEN SYNDROME)IS GENETICALLY HETEROGENEOUS
Authors: SCHULZEBAHR E HAVERKAMP W WEDEKIND H RUBIE C HORDT M BORGGREFE M ASSMANN G BREITHARDT G FUNKE H
Citation: E. Schulzebahr et al., AUTOSOMAL RECESSIVE LONG-QT SYNDROME (JERVELL LANGE-NIELSEN SYNDROME)IS GENETICALLY HETEROGENEOUS, Human genetics, 100(5-6), 1997, pp. 573-576
IDENTIFICATION OF A NEW GENE FOR AUTOSOMAL RECESSIVE LONG-CT SYNDROME(JERVELL-LANGE-NIELSEN-SYNDROME)
Authors: SCHULZEBAHR E WANG Q HAVERKAMP W WEDEKIND H RUBIE C CHEN QY HORDT M BREITHARDT G FUNKE H
Citation: E. Schulzebahr et al., IDENTIFICATION OF A NEW GENE FOR AUTOSOMAL RECESSIVE LONG-CT SYNDROME(JERVELL-LANGE-NIELSEN-SYNDROME), Circulation, 96(8), 1997, pp. 308-308
DO MUTATIONS IN CARDIAC ION-CHANNEL GENES PREDISPOSE TO DRUG-INDUCED (ACQUIRED) LONG-QT SYNDROME
Authors: SCHULZEBAHR E HAVERKAMP W HORDT M WEDEKIND H BORGGREFE M FUNKE H
Citation: E. Schulzebahr et al., DO MUTATIONS IN CARDIAC ION-CHANNEL GENES PREDISPOSE TO DRUG-INDUCED (ACQUIRED) LONG-QT SYNDROME, Circulation, 96(8), 1997, pp. 1167-1167
GENE WITH GENE INTERACTION INFLUENCES THE EXPRESSIVITY IN CHROMOSOME 11-SPECIFIC (KVLQT1) LONG-QT SYNDROME IN A LARGE GERMAN KINDRED
Authors: WEDEKIND H SCHULZEBAHR E HAVERKAMP W HORDT M LANGE S RUBLE C BORGGREFE M FUNKE H
Citation: H. Wedekind et al., GENE WITH GENE INTERACTION INFLUENCES THE EXPRESSIVITY IN CHROMOSOME 11-SPECIFIC (KVLQT1) LONG-QT SYNDROME IN A LARGE GERMAN KINDRED, Circulation, 96(8), 1997, pp. 1171-1171
IDENTIFICATION AND FUNCTIONAL-CHARACTERIZATION OF A NOVEL GENE FOR AUTOSOMAL RECESSIVE DEAFNESS AND LONG-QT SYNDROME (JERVELL AND LANGE-NIELSEN-SYNDROME)
Authors: SCHULZEBAHR E WANG Q WEDEKIND H HAVERKAMP W CHEN Q SUN Y RUBIE C HORDT M TOWBIN JA BORGGREFE M ASSMANN G QU X SOMBERG JC BREITHARDT G OBERTI C FUNKE H
Citation: E. Schulzebahr et al., IDENTIFICATION AND FUNCTIONAL-CHARACTERIZATION OF A NOVEL GENE FOR AUTOSOMAL RECESSIVE DEAFNESS AND LONG-QT SYNDROME (JERVELL AND LANGE-NIELSEN-SYNDROME), American journal of human genetics, 61(4), 1997, pp. 48-48
A SEVERE FORM OF LONG-QT SYNDROME CAUSED BY 2 KVLQT1 MUTATIONS LOCATED IN CIS
Authors: WEDEKIND H SCHULZEBAHR E LANGE S RUBIE C HAVERKAMP W HORDT M BORGGREFE M ASSMANN G BREITHARDT G FUNKE H
Citation: H. Wedekind et al., A SEVERE FORM OF LONG-QT SYNDROME CAUSED BY 2 KVLQT1 MUTATIONS LOCATED IN CIS, American journal of human genetics, 61(4), 1997, pp. 2051-2051
FREQUENCY AND PHENOTYPE OF HERG MUTATIONS IN CONGENITAL LONG QT SYNDROME (LQTS)
Authors: SCHULZEBAHR E HAVERKAMP W WIEBUSCH H WEDEKIND H HORDT M BORGGREFE M BREITHARDT G FUNKE H
Citation: E. Schulzebahr et al., FREQUENCY AND PHENOTYPE OF HERG MUTATIONS IN CONGENITAL LONG QT SYNDROME (LQTS), Circulation, 94(8), 1996, pp. 4205-4205
DIETARY INFLUENCES ON PRODUCT QUALITY IN AFRICAN CATFISH (CLARIAS-GARIEPINUS)
Authors: WEDEKIND H
Citation: H. Wedekind, DIETARY INFLUENCES ON PRODUCT QUALITY IN AFRICAN CATFISH (CLARIAS-GARIEPINUS), Journal of applied ichthyology, 11(3-4), 1995, pp. 347-353
COMMUNICATION SUPPORT FOR COOPERATIVE WORK
Authors: KIRSCHE T LENZ R LUHRSEN H MEYERWEGENER K WEDEKIND H BEVER M SCHAFFER U SCHOTTMULLER C
Citation: T. Kirsche et al., COMMUNICATION SUPPORT FOR COOPERATIVE WORK, Computer communications, 16(9), 1993, pp. 594-602
MAPPING OF A GENE FOR FAMILIAL JUVENILE NEPHRONOPHTHISIS REFINING THEMAP AND DEFINING FLANKING MARKERS ON CHROMOSOME-2
Authors: HILDEBRANDT F SINGHSAWHNEY I SCHNIEDERS B CENTOFANTE L OMRAN H POHLMANN A SCHMALTZ C WEDEKIND H SCHUBOTZ C ANTIGNAC C WEBER JL BRANDIS M
Citation: F. Hildebrandt et al., MAPPING OF A GENE FOR FAMILIAL JUVENILE NEPHRONOPHTHISIS REFINING THEMAP AND DEFINING FLANKING MARKERS ON CHROMOSOME-2, American journal of human genetics, 53(6), 1993, pp. 1256-1261
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