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Results: 1-17 |
Results: 17
AN INCREASED FREQUENCY OF NUMERICAL CHROMOSOMAL-ABNORMALITIES AND 1P36 DELETIONS IN ISOLATED CELLS FROM PARAFFIN SECTIONS OF MALIGNANT MELANOMAS BY MEANS OF INTERPHASE CYTOGENETICS
Authors: POETSCH M WOENCKHAUS C DITTBERNER T PAMBOR M LORENZ G HERRMANN FH
Citation: M. Poetsch et al., AN INCREASED FREQUENCY OF NUMERICAL CHROMOSOMAL-ABNORMALITIES AND 1P36 DELETIONS IN ISOLATED CELLS FROM PARAFFIN SECTIONS OF MALIGNANT MELANOMAS BY MEANS OF INTERPHASE CYTOGENETICS, Cancer genetics and cytogenetics, 104(2), 1998, pp. 146-152
DIFFERENCES IN CHROMOSOMAL-ABERRATIONS BETWEEN NODULAR AND SUPERFICIAL SPREADING MALIGNANT-MELANOMA DETECTED BY INTERPHASE CYTOGENETICS
Authors: POETSCH M WOENCKHAUS C DITTBERNER T PAMBOR M LORENZ G HERRMANN FH
Citation: M. Poetsch et al., DIFFERENCES IN CHROMOSOMAL-ABERRATIONS BETWEEN NODULAR AND SUPERFICIAL SPREADING MALIGNANT-MELANOMA DETECTED BY INTERPHASE CYTOGENETICS, Laboratory investigation, 78(7), 1998, pp. 883-888
A DE-NOVO TRANSLOCATION 46,X,T(X-15) CAUSING HEMOPHILIA-B IN A GIRL -A CASE-REPORT
Authors: SCHRODER W POETSCH M GAZDA H WERNER W REICHELT T KNOLL W ROKICKAMILEWSKA R ZIELENIEWSKA B HERRMANN FH
Citation: W. Schroder et al., A DE-NOVO TRANSLOCATION 46,X,T(X-15) CAUSING HEMOPHILIA-B IN A GIRL -A CASE-REPORT, British Journal of Haematology, 100(4), 1998, pp. 750-757
IN-VIVO EVIDENCE FOR COMPROMISED PHENYLALANINE METABOLISM IN VITILIGO
Authors: SCHALLREUTER KU ZSCHIESCHE M MOORE J PANSKE A HIBBERTS NA HERRMANN FH METELMANN HR SAWATZKI J
Citation: Ku. Schallreuter et al., IN-VIVO EVIDENCE FOR COMPROMISED PHENYLALANINE METABOLISM IN VITILIGO, Biochemical and biophysical research communications, 243(2), 1998, pp. 395-399
6 NOVEL MUTATIONS IN THE EMERIN GENE CAUSING X-LINKED EMERY-DREIFUSS-MUSCULAR-DYSTROPHY
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
PREVALENCE OF FACTOR-V-LEIDEN MUTATION IN VARIOUS POPULATIONS
Authors: HERRMANN FH KOESLING M SCHRODER W ALTMAN R BONILLA RJ LOPACIUK S PEREZREQUEJO JL SINGH JR
Citation: Fh. Herrmann et al., PREVALENCE OF FACTOR-V-LEIDEN MUTATION IN VARIOUS POPULATIONS, Genetic epidemiology, 14(4), 1997, pp. 403-411
A DE-NOVO TRANSLOCATION T(X-15) RESULTS IN THE EXPRESSION OF HEMOPHILIA-B IN A GIRL
Authors: SCHRODER W GAZDA H POETSCH M WERNER W KNOLL W ROKICKAMILEWSKA R ZIELENIEWSKA B HERRMANN FH
Citation: W. Schroder et al., A DE-NOVO TRANSLOCATION T(X-15) RESULTS IN THE EXPRESSION OF HEMOPHILIA-B IN A GIRL, Thrombosis and haemostasis, 1997, pp. 945-945
CHARACTERIZATION OF THE MOLECULAR DEFECTS OF THE FVII GENE IN FACTOR-VII DEFICIENCY
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
HEMOPHILIA-B IN FEMALE TWINS CAUSED BY A POINT MUTATION IN ONE FACTOR-IX GENE AND NONRANDOM INACTIVATION PATTERNS OF THE X-CHROMOSOMES
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
DIRECT MOLECULAR-GENETIC DIAGNOSIS AND HETEROZYGOTE IDENTIFICATION INX-LINKED EMERY-DREIFUSS MUSCULAR-DYSTROPHY BY HETERODUPLEX ANALYSIS
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
LARGE-SCALE SCREENING FOR FACTOR-V LEIDEN MUTATION IN A NORTH-EASTERNGERMAN POPULATION
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
WORLD DISTRIBUTION OF FACTOR-V LEIDEN MUTATION
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
INTRON-22 OF FACTOR-VIII GENE - A HOT-SPOT FOR STRUCTURAL-ABERRATIONSCAUSING SEVERE HEMOPHILIA-A
Authors: SCHRODER W WEHNERT M HERRMANN FH
Citation: W. Schroder et al., INTRON-22 OF FACTOR-VIII GENE - A HOT-SPOT FOR STRUCTURAL-ABERRATIONSCAUSING SEVERE HEMOPHILIA-A, Blood, 87(7), 1996, pp. 3067-3068
25 NOVEL MUTATIONS OF THE FACTOR-IX GENE IN HEMOPHILIA-B
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
INVERSION SCREENING IN PATIENTS WITH SEVERE HEMOPHILIA
Authors: SCHRODER AW WEHNERT M HERRMANN FH
Citation: Aw. Schroder et al., INVERSION SCREENING IN PATIENTS WITH SEVERE HEMOPHILIA, Thrombosis and haemostasis, 73(6), 1995, pp. 1218-1218
MOLECULAR DEFECTS AND GENOMIC DIAGNOSIS OF HEMOPHILIA-B
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
MUTATIONS OF THE IDURONATE-2-SULFATASE (IDS) GENE IN PATIENTS WITH HUNTER-SYNDROME (MUCOPOLYSACCHARIDOSIS-II)
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
Risultati: 1-17 |