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Results: 1-13 |
Results: 13

Authors: WAGNER K SCHNEDITZ P ROSENKRANZ W
Citation: K. Wagner et al., A NEW FRAMESHIFT MUTATION 460DELG IN EXON-4 OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR) GENE, Human mutation, 7(2), 1996, pp. 183-183

Authors: WAGNER K KROISEL PM ROSENKRANZ W
Citation: K. Wagner et al., PREPARATIVE IN-SITU HYBRIDIZATION (PREP-ISH) OF A CDNA LIBRARY CORRESPONDING TO SUBREGIONS OF CHROMOSOME 7P, Cytogenetics and cell genetics, 71(1), 1995, pp. 24-24

Authors: GREIL I WAGNER K EBER E ZACH M ROSENKRANZ W
Citation: I. Greil et al., MOLECULAR AND CLINICAL FINDINGS IN AUSTRI AN CYSTIC-FIBROSIS PATIENTSWITH MUTATIONS IN EXON 11 OF THE CFTR GENE, Wiener Klinische Wochenschrift, 107(15), 1995, pp. 464-469

Authors: WAGNER K GREIL I SCHNEDITZ P POMMER M ROSENKRANZ W
Citation: K. Wagner et al., A CYSTIC-FIBROSIS PATIENT WITH DELTA-F508, G542X AND A DELETION AT THE D7S8 LOCUS, Human mutation, 3(3), 1994, pp. 327-329

Authors: ORTH U ROSENKRANZ W SCHWINGER E GAL A
Citation: U. Orth et al., LINKAGE ANALYSIS IN FAMILIES WITH LOWE SYNDROME MAPS OCRL DISTAL TO DXS42, Cytogenetics and cell genetics, 67(4), 1994, pp. 346-346

Authors: KROISEL PM WAGNER K GREEN ED GUAN XY MELTZER PS DEJONG P ROSENKRANZ W
Citation: Pm. Kroisel et al., ANALYSIS OF THE 7P11-]14 REGION USING MICRODISSECTION LIBRARIES, Cytogenetics and cell genetics, 65(1-2), 1994, pp. 69-70

Authors: REISECKER F LEBLHUBER F LEXNER R RADNER G ROSENKRANZ W WAGNER K
Citation: F. Reisecker et al., A SPORADIC FORM OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - CLINICAL, ELECTRODIAGNOSTIC, AND MOLECULAR-GENETIC FINDINGS, Neurology, 44(4), 1994, pp. 753-755

Authors: ROSENKRANZ W GRUNDMANN E
Citation: W. Rosenkranz et E. Grundmann, IMMUNOMODULATING EFFECT OF LIVING NONPATH OGENIC ENTEROCOCCUS-FAECALIS ORIGINATED FROM HUMANS, Arzneimittel-Forschung, 44-1(5), 1994, pp. 691-695

Authors: GREIL I WAGNER K ROSENKRANZ W
Citation: I. Greil et al., A NEW MISSENSE MUTATION-G1249E IN EXON-20 OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR) GENE, Human heredity, 44(4), 1994, pp. 238-240

Authors: WAGNER K GREIL I SCHNEDITZ P ROSENKRANZ W
Citation: K. Wagner et al., A NEW MISSENSE MUTATION G126D IN EXON-4 OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR) GENE, Human heredity, 44(1), 1994, pp. 56-57

Authors: GREIL I WAGNER K ROSENKRANZ W
Citation: I. Greil et al., IDENTIFICATION OF A NEW SPLICE-SITE MUTATION (3849-]A) IN THE INTRON-19 OF THE CFTR GENE(1G), Human molecular genetics, 2(12), 1993, pp. 2171-2172

Authors: ORTH U ROSENKRANZ W SCHWINGER E HOLZGREVE W GAL A
Citation: U. Orth et al., MOLECULAR-GENETIC DIAGNOSTICS FOR WISCOTT -ALDRICH SYNDROME, Monatsschrift fur Kinderheilkunde, 141(9), 1993, pp. 728-731

Authors: ROSENKRANZ W
Citation: W. Rosenkranz, THRESHOLD OPTIMIZATION OF A DIGITAL FM DEMODULATOR WITH BASEBAND-PLL, Frequenz, 47(5-6), 1993, pp. 166-173
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