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Results: 1-25 | 26-36 |
Results: 26-36/36
A RECURRENT 14-BP DELETION IN THE CLCN1 GENE ASSOCIATED WITH GENERALIZED MYOTONIA (BECKER)
Authors: MEYERKLEINE C RICKER K OTTO M KOCH MC
Citation: C. Meyerkleine et al., A RECURRENT 14-BP DELETION IN THE CLCN1 GENE ASSOCIATED WITH GENERALIZED MYOTONIA (BECKER), Human molecular genetics, 3(6), 1994, pp. 1015-1016
BRAIN DISEASE AND MOLECULAR ANALYSIS IN MYOTONIC-DYSTROPHY
Authors: DAMIAN MS BACHMANN G KOCH MC SCHILLING G STOPPLER S DORNDORF W
Citation: Ms. Damian et al., BRAIN DISEASE AND MOLECULAR ANALYSIS IN MYOTONIC-DYSTROPHY, NeuroReport, 5(18), 1994, pp. 2549-2552
MOLECULAR AND GENETIC-CHARACTERIZATION OF GERMAN FAMILIES WITH PARAMYOTONIA-CONGENITA AND DEMONSTRATION OF FOUNDER EFFECT IN THE RAVENSBERGFAMILIES
Authors: MEYERKLEINE C OTTO M ZOLL B KOCH MC
Citation: C. Meyerkleine et al., MOLECULAR AND GENETIC-CHARACTERIZATION OF GERMAN FAMILIES WITH PARAMYOTONIA-CONGENITA AND DEMONSTRATION OF FOUNDER EFFECT IN THE RAVENSBERGFAMILIES, Human genetics, 93(6), 1994, pp. 707-710
MAPPING AND CHARACTERIZATION OF THE GENE FOR HUMAN MYOTONIA
Authors: KOCH MC STEINMEYER K OTTO M LORENZ C MEYERKLEINE C RICKER K JENTSCH TJ
Citation: Mc. Koch et al., MAPPING AND CHARACTERIZATION OF THE GENE FOR HUMAN MYOTONIA, Cytogenetics and cell genetics, 65(1-2), 1994, pp. 71-71
MULTIMERIC STRUCTURE OF CLC-1 CHLORIDE CHANNEL REVEALED BY MUTATIONS IN DOMINANT MYOTONIA-CONGENITA (THOMSEN)
Authors: STEINMEYER K LORENZ C PUSCH M KOCH MC JENTSCH TJ
Citation: K. Steinmeyer et al., MULTIMERIC STRUCTURE OF CLC-1 CHLORIDE CHANNEL REVEALED BY MUTATIONS IN DOMINANT MYOTONIA-CONGENITA (THOMSEN), EMBO journal, 13(4), 1994, pp. 737-743
MIXED AXONAL-DEMYELINATING POLYNEUROPATHY AS PREDOMINANT MANIFESTATION OF MYOTONIC-DYSTROPHY
Authors: VONGIESEN HJ STOLL G KOCH MC BENECKE R
Citation: Hj. Vongiesen et al., MIXED AXONAL-DEMYELINATING POLYNEUROPATHY AS PREDOMINANT MANIFESTATION OF MYOTONIC-DYSTROPHY, Muscle & nerve, 17(6), 1994, pp. 701-703
PROXIMAL MYOTONIC MYOPATHY - A NEW DOMINANT DISORDER WITH MYOTONIA, MUSCLE WEAKNESS, AND CATARACTS
Authors: RICKER K KOCH MC LEHMANNHORN F PONGRATZ D OTTO M HEINE R MOXLEY RT
Citation: K. Ricker et al., PROXIMAL MYOTONIC MYOPATHY - A NEW DOMINANT DISORDER WITH MYOTONIA, MUSCLE WEAKNESS, AND CATARACTS, Neurology, 44(8), 1994, pp. 1448-1452
DE-NOVO FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY DEFINED BY DNA-PROBE P13E-11 (D4F104S1)
Authors: JARDINE PE KOCH MC LUNT P MAYNARD J BATHKE KD HARPER PS UPADHYAYA M
Citation: Pe. Jardine et al., DE-NOVO FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY DEFINED BY DNA-PROBE P13E-11 (D4F104S1), Archives of Disease in Childhood, 71(3), 1994, pp. 221-227
CHARACTERISTICS OF INTERGENERATIONAL CONTRACTIONS OF THE CTG REPEAT IN MYOTONIC-DYSTROPHY
Authors: ASHIZAWA T ANVRET M BAIGET M BARCELO JM BRUNNER H COBO AM DALLAPICCOLA B FENWICK RG GRANDELL U HARLEY H JUNIEN C KOCH MC KORNELUK RG LAVEDAN C MIKI T MULLEY JC DEMUNAIN AL NOVELLI G ROSES AD SELTZER WK SHAW DJ SMEETS H SUTHERLAND GR YAMAGATA H HARPER PS
Citation: T. Ashizawa et al., CHARACTERISTICS OF INTERGENERATIONAL CONTRACTIONS OF THE CTG REPEAT IN MYOTONIC-DYSTROPHY, American journal of human genetics, 54(3), 1994, pp. 414-423
MAJOR SKELETAL-MUSCLE CHLORIDE CHANNEL CLC-1 AND ITS INVOLVEMENT IN MYOTONIA
Authors: STEINMEYER K ORTLAND C KLOCKE R GRONEMEIER M JOCKUSCH H LORENZ C SCHMEKAL C KOCH MC JENTSCH TJ
Citation: K. Steinmeyer et al., MAJOR SKELETAL-MUSCLE CHLORIDE CHANNEL CLC-1 AND ITS INVOLVEMENT IN MYOTONIA, Journal of muscle research and cell motility, 14(2), 1993, pp. 230-230
EVIDENCE FOR GENETIC HOMOGENEITY IN AUTOSOMAL RECESSIVE GENERALIZED MYOTONIA (BECKER)
Authors: KOCH MC RICKER K OTTO M WOLF F ZOLL B LORENZ C STEINMEYER K JENTSCH TJ
Citation: Mc. Koch et al., EVIDENCE FOR GENETIC HOMOGENEITY IN AUTOSOMAL RECESSIVE GENERALIZED MYOTONIA (BECKER), Journal of Medical Genetics, 30(11), 1993, pp. 914-917
Risultati: 1-25 | 26-36 |