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Results:
1-21
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Results: 21
Authors:
FECHNER PU
SINGH D
WULFF K
Citation: Pu. Fechner et al., IRIS-CLAW LENS IN PHAKIC EYES TO CORRECT HYPEROPIA - PRELIMINARY-STUDY, Journal of cataract and refractive surgery, 24(1), 1998, pp. 48-56
Authors:
MEISEL P
WELLE J
SIEGMUND W
WULFF K
FENGLER JD
Citation: P. Meisel et al., ASSOCIATION BETWEEN POLYMORPHISMS OF THE N-ACETYLTRANSFERASE (NAT2) GENE AND BILIRUBIN UDP-GLUCURONOSYL-TRANSFERASE GENE IN PATIENTS WITH GILBERTS-SYNDROME, Naunyn-Schmiedeberg's archives of pharmacology, 357(4), 1998, pp. 661-661
Authors:
HALONEN P
CLERC P
GOWARD T
BRODO IM
WULFF K
Citation: P. Halonen et al., SYNOPSIS OF THE GENUS USNEA (LICHENIZED ASCOMYCETES) IN BRITISH-COLUMBIA, CANADA, The Bryologist, 101(1), 1998, pp. 36-60
Authors:
WULFF K
FECHNER PU
Citation: K. Wulff et Pu. Fechner, HERPES-SIMPLEX KERATITIS AFTER PHOTOREFRACTIVE KERATECTOMY, Journal of refractive surgery, 13(7), 1997, pp. 613-613
Authors:
WULFF K
PARRISH JE
HERRMANN FH
WEHNERT M
Citation: K. Wulff et al., 6 NOVEL MUTATIONS IN THE EMERIN GENE CAUSING X-LINKED EMERY-DREIFUSS-MUSCULAR-DYSTROPHY, Human mutation, 9(6), 1997, pp. 526-530
Authors:
MEISEL P
SCHROEDER C
WULFF K
SIEGMUND W
Citation: P. Meisel et al., RELATIONSHIP BETWEEN HUMAN GENOTYPE AND PHENOTYPE OF N-ACETYLTRANSFERASE (NAT2) AS ESTIMATED BY DISCRIMINANT-ANALYSIS AND MULTIPLE LINEAR-REGRESSION .1. GENOTYPE AND N-ACETYLATION IN-VIVO, Pharmacogenetics, 7(3), 1997, pp. 241-246
Authors:
HERRMANN FH
WULFF K
Citation: Fh. Herrmann et K. Wulff, CHARACTERIZATION OF THE MOLECULAR DEFECTS OF THE FVII GENE IN FACTOR-VII DEFICIENCY, Thrombosis and haemostasis, 1997, pp. 1688-1688
Authors:
SCHRODER W
WULFF K
WOLLINA K
HERRMANN FH
Citation: W. Schroder et al., HEMOPHILIA-B IN FEMALE TWINS CAUSED BY A POINT MUTATION IN ONE FACTOR-IX GENE AND NONRANDOM INACTIVATION PATTERNS OF THE X-CHROMOSOMES, Thrombosis and haemostasis, 78(5), 1997, pp. 1347-1351
Authors:
WULFF K
EBENER U
WEHNERT CS
WARD PA
REUNER U
HIEBSCH W
HERRMANN FH
WEHNERT M
Citation: K. Wulff et al., DIRECT MOLECULAR-GENETIC DIAGNOSIS AND HETEROZYGOTE IDENTIFICATION INX-LINKED EMERY-DREIFUSS MUSCULAR-DYSTROPHY BY HETERODUPLEX ANALYSIS, Disease markers, 13(2), 1997, pp. 77-86
Authors:
SCHRODER W
KOESLING M
WULFF K
WEHNERT M
HERRMANN FH
Citation: W. Schroder et al., LARGE-SCALE SCREENING FOR FACTOR-V LEIDEN MUTATION IN A NORTH-EASTERNGERMAN POPULATION, Haemostasis, 26(5), 1996, pp. 233-236
Authors:
WULFF K
WENZEL J
SEILER T
Citation: K. Wulff et al., LONG-TERM RESULTS OF PHOTOREFRACTIVE KERATECTOMY (PRK) - 5-YEAR FOLLOW-UP, Investigative ophthalmology & visual science, 37(3), 1996, pp. 2593-2593
Authors:
SCHRODER W
KOESSLING M
WULFF K
WEHNERT M
HERRMANN FH
Citation: W. Schroder et al., WORLD DISTRIBUTION OF FACTOR-V LEIDEN MUTATION, Lancet, 347(8993), 1996, pp. 58-59
Authors:
WULFF K
SCHRODER W
WEHNERT M
HERRMANN FH
Citation: K. Wulff et al., 25 NOVEL MUTATIONS OF THE FACTOR-IX GENE IN HEMOPHILIA-B, Human mutation, 6(4), 1995, pp. 346-348
Authors:
HERRMANN FH
WULFF K
SCHRODER W
Citation: Fh. Herrmann et al., MOLECULAR DEFECTS AND GENOMIC DIAGNOSIS OF HEMOPHILIA-B, Thrombosis and haemostasis, 73(6), 1995, pp. 1221-1221
Authors:
PETERSEN MB
BRONDUMNIELSEN K
HANSEN LK
WULFF K
Citation: Mb. Petersen et al., CLINICAL, CYTOGENETIC, AND MOLECULAR DIAGNOSIS OF ANGELMAN SYNDROME -ESTIMATED PREVALENCE RATE IN A DANISH COUNTY, American journal of medical genetics, 60(3), 1995, pp. 261-262
Authors:
SCHRODER W
WULFF K
WEHNERT M
SEIDLITZ G
HERRMANN FH
Citation: W. Schroder et al., MUTATIONS OF THE IDURONATE-2-SULFATASE (IDS) GENE IN PATIENTS WITH HUNTER-SYNDROME (MUCOPOLYSACCHARIDOSIS-II), Human mutation, 4(2), 1994, pp. 128-131
Authors:
GERDES AM
PETERSEN MB
SCHRODER HD
WULFF K
BRONDUMNIELSEN K
Citation: Am. Gerdes et al., CONGENITAL MYOPATHY WITH FIBER-TYPE DISPROPORTION - A FAMILY WITH A CHROMOSOMAL TRANSLOCATION T(1017) MAY INDICATE CANDIDATE GENE REGIONS, Clinical genetics, 45(1), 1994, pp. 11-16
Authors:
KAMPER J
WULFF K
Citation: J. Kamper et K. Wulff, EARLY CPAP MINIMAL HANDLING, Acta paediatrica, 82(10), 1993, pp. 900-900
Authors:
HANSEN LK
WULFF K
DORCHE C
CHRISTENSEN E
Citation: Lk. Hansen et al., MOLYBDENUM COFACTOR DEFICIENCY IN 2 SIBLINGS - DIAGNOSTIC DIFFICULTIES, European journal of pediatrics, 152(8), 1993, pp. 662-664
Authors:
BRONDUMNIELSEN K
BAJALICA S
WULFF K
MIKKELSEN M
Citation: K. Brondumnielsen et al., CHROMOSOME PAINTING USING FISH (FLUORESCENCE IN-SITU HYBRIDIZATION) WITH CHROMOSOME-6-SPECIFIC LIBRARY DEMONSTRATES THE ORIGIN OF A DE-NOVO6Q+ MARKER CHROMOSOME, Clinical genetics, 43(5), 1993, pp. 235-239
Authors:
PETERSEN MB
TOMMERUP N
ORSTAVIK KH
WULFF K
SORENSEN JC
MIKKELSEN M
Citation: Mb. Petersen et al., MOLECULAR ANALYSIS OF FAMILIAL PRADER-WILLI-SYNDROME, American journal of human genetics, 53(3), 1993, pp. 1749-1749
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1-21
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