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Results: 1-9 |
Results: 9
DISCOURSE MARKERS AND GLOBAL COHERENCE IN CONVERSATION
Authors: LENK U
Citation: U. Lenk, DISCOURSE MARKERS AND GLOBAL COHERENCE IN CONVERSATION, Journal of pragmatics, 30(2), 1998, pp. 245-257
4 NEW POLYMORPHISMS IN THE HUMAN DYSTROPHIN GENE FROM AN ARGENTINEAN POPULATION
Authors: BARANZINI SE LENK U SZIJAN I SPEER A
Citation: Se. Baranzini et al., 4 NEW POLYMORPHISMS IN THE HUMAN DYSTROPHIN GENE FROM AN ARGENTINEAN POPULATION, Muscle & nerve, 20(11), 1997, pp. 1451-1453
LANGUAGE AND POWER IN THE OFFICE - PSCHAI D,P
Authors: LENK U BUBLITZ W
Citation: U. Lenk et W. Bublitz, LANGUAGE AND POWER IN THE OFFICE - PSCHAI D,P, Zeitschrift fur Anglistik und Amerikanistik, 45(1), 1997, pp. 78-79
A CYSTEINE-3340 SUBSTITUTION IN THE DYSTROGLYCAN-BINDING DOMAIN OF DYSTROPHIN-ASSOCIATED WITH DUCHENNE MUSCULAR-DYSTROPHY, MENTAL-RETARDATION AND ABSENCE OF THE ERG B-WAVE
Authors: LENK U OEXLE K VOIT T ANCKER U HELLNER KA SPEER A HUBNER C
Citation: U. Lenk et al., A CYSTEINE-3340 SUBSTITUTION IN THE DYSTROGLYCAN-BINDING DOMAIN OF DYSTROPHIN-ASSOCIATED WITH DUCHENNE MUSCULAR-DYSTROPHY, MENTAL-RETARDATION AND ABSENCE OF THE ERG B-WAVE, Human molecular genetics, 5(7), 1996, pp. 973-975
PROTEIN TRUNCATION TEST - ANALYSIS OF 2 NOVEL POINT MUTATIONS AT THE CARBOXY-TERMINUS OF THE HUMAN DYSTROPHIN GENE ASSOCIATED WITH MENTAL-RETARDATION
Authors: TUFFERY S LENK U ROBERTS RG COUBES C DEMAILLE J CLAUSTRES M
Citation: S. Tuffery et al., PROTEIN TRUNCATION TEST - ANALYSIS OF 2 NOVEL POINT MUTATIONS AT THE CARBOXY-TERMINUS OF THE HUMAN DYSTROPHIN GENE ASSOCIATED WITH MENTAL-RETARDATION, Human mutation, 6(2), 1995, pp. 126-135
STUDIES OF THE CODING REGION OF THE NEURONAL GLUTAMATE TRANSPORTER GENE IN AMYOTROPHIC-LATERAL-SCLEROSIS
Authors: MEYER T LENK U KUTHER G WEINDL A SPEER A LUDOLPH AC
Citation: T. Meyer et al., STUDIES OF THE CODING REGION OF THE NEURONAL GLUTAMATE TRANSPORTER GENE IN AMYOTROPHIC-LATERAL-SCLEROSIS, Annals of neurology, 37(6), 1995, pp. 817-839
CARRIER DETECTION IN DMD FAMILIES WITH POINT MUTATIONS, USING PCR-SSCP AND DIRECT SEQUENCING
Authors: LENK U HANKE R SPEER A
Citation: U. Lenk et al., CARRIER DETECTION IN DMD FAMILIES WITH POINT MUTATIONS, USING PCR-SSCP AND DIRECT SEQUENCING, Neuromuscular disorders, 4(5-6), 1994, pp. 411-418
POINT MUTATIONS AT THE CARBOXY-TERMINUS OF THE HUMAN DYSTROPHIN GENE - IMPLICATIONS FOR AN ASSOCIATION WITH MENTAL-RETARDATION IN DMD PATIENTS
Authors: LENK U HANKE R THIELE H SPEER A
Citation: U. Lenk et al., POINT MUTATIONS AT THE CARBOXY-TERMINUS OF THE HUMAN DYSTROPHIN GENE - IMPLICATIONS FOR AN ASSOCIATION WITH MENTAL-RETARDATION IN DMD PATIENTS, Human molecular genetics, 2(11), 1993, pp. 1877-1881
NONISOTOPIC ANALYSIS OF SINGLE-STRAND CONFORMATION POLYMORPHISM (SSCP) IN THE EXON-13 REGION OF THE HUMAN DYSTROPHIN GENE
Authors: LENK U HANKE R KRAFT U GRADE K GRUNEWALD I SPEER A
Citation: U. Lenk et al., NONISOTOPIC ANALYSIS OF SINGLE-STRAND CONFORMATION POLYMORPHISM (SSCP) IN THE EXON-13 REGION OF THE HUMAN DYSTROPHIN GENE, Journal of Medical Genetics, 30(11), 1993, pp. 951-954
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