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51

Structural gene aberrations in mucopolysaccharidosis II (Hunter)

Manfred Wehnert, John J. Hopwood, Winnie Schröder, Falko H. Herrmann

Journal:

Year:

1992

Language:

english

File:

PDF, 435 KB

english, 1992

52

Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome

G. Camp, H. Backhovens, M. Cruts, A. Wehnert, W. Hul, P. Stinissen, C. Broeckhoven

Journal:

Year:

1991

Language:

english

File:

PDF, 542 KB

english, 1991

53

Subregional localization of the chromosome 21 loci D21S24 and D21S26 using physical mapping techniques

Wim Hul, Hubert Backhovens, Guy Camp, Piet Stinissen, Marc Cruts, Anita Wehnert, Christine Broeckhoven

Journal:

Year:

1991

Language:

english

File:

PDF, 508 KB

english, 1991

54

A new marker at DXS 115 useful for carrier detection in hemophilia A

Manfred Wehnert, Winnie Schröder, Falko H. Herrmann

Journal:

Year:

1990

Language:

english

File:

PDF, 251 KB

english, 1990

55

Reply to the letter by Kling et al.

Manfred Wehnert, Winnie Schröder, Falko H. Herrmann

Journal:

Year:

1992

Language:

english

File:

PDF, 125 KB

english, 1992

56

Book reviews

P. P. Jauhar, M. Wehnert, H. -D. Görtz, D. Gröger Halle, A. M. Harten, J. F. G. M. Wintermans, P. Eberle, G. Machill

Journal:

Theoretical and Applied Genetics

Year:

1992

Language:

english

File:

PDF, 438 KB

english, 1992

57

Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndrome

Guy Camp, Piet Stinissen, Wim Hul, Hubert Backhovens, Anita Wehnert, Antoon Vandenberge, Christine Broeckhoven

Journal:

Year:

1989

Language:

english

File:

PDF, 463 KB

english, 1989

58

Linkage analysis of the Duffy blood group marker with several chromosome 1 genes in an extended pedigree with Charcot-Marie-Tooth disease

Peter Raeymaekers, Christine Broeckhoven, Hubert Backhovens, Anita Wehnert, Ludo Muylle, Peter Jonghe, Jan Ghenens, Jean-Jacques Martin, Antoon Vandenberghe

Journal:

Year:

1989

Language:

english

File:

PDF, 281 KB

english, 1989

59

Book reviews

H. F. Linskens, W. E. Crusio, M. Wehnert

Journal:

Theoretical and Applied Genetics

Year:

1989

Language:

english

File:

PDF, 142 KB

english, 1989

60

The Duffy blood group is linked to the α-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1

Peter Raeymaekers, Christine Broeckhoven, Hubert Backhovens, Anita Wehnert, Ludo Muylle, Peter Jonghe, Jan Gheuens, Antoon Vandenberghe

Journal:

Year:

1988

Language:

english

File:

PDF, 295 KB

english, 1988

61

Reliability of the Tønnesen technique for the identification of Hunter carriers

L. Petruschka, G. Machill, M. Wehnert, G. Seidlitz, A. Knapp

Journal:

Year:

1983

Language:

english

File:

PDF, 256 KB

english, 1983

62

Genetic complementation analysis in somatic cell hybrids of α-L-iduronidase deficient cells

M. Wehnert, G. Machill, L. Petruschka

Journal:

Year:

1985

Language:

english

File:

PDF, 80 KB

english, 1985

63

Book reviews

J. A. M. Mey, Inés Noher Halac, H. F. Linskens, L. Petruschka, M. Wehnert

Journal:

Theoretical and Applied Genetics

Year:

1988

Language:

english

File:

PDF, 368 KB

english, 1988

64

Deletion screening in patients with Duchenne muscular dystrophy

K. Wulff, F. H. Herrmann, M. C. Wapenaar, M. Wehnert

Journal:

Journal of Neurology

Year:

1989

Language:

english

File:

PDF, 439 KB

english, 1989

65

Study of hexosaminidase isozyme reconstruction during hybridization of fibroblasts from patients with Tay-Sachs' and Sandhoff's diseases

E. M. Beier, G. Ya. Wiederschain, M. Wehnert

Journal:

Bulletin of Experimental Biology and Medicine

Year:

1984

Language:

english

File:

PDF, 643 KB

english, 1984

66

Glucose oxidase immobilized on eupergit C and CPG-10 a comparison

G. Wehnert, A. Sauerbrei, K. Schügerl

Journal:

Biotechnology Letters

Year:

1985

Language:

english

File:

PDF, 182 KB

english, 1985

67

Characterization of three new deletions at the 5′ end of the HPRT structural gene

M. Wehnert, F. H. Herrmann

Journal:

Journal of Inherited Metabolic Disease

Year:

1990

Language:

english

File:

PDF, 1.17 MB

english, 1990

68

New technical possibilities for simultaneous cystometry

J. Wehnert, R. Werthschützky

Journal:

International Urology and Nephrology

Year:

1980

Language:

english

File:

PDF, 501 KB

english, 1980

69

Assessment of the regional lymph node status in radiation monotherapy of prostatic cancer

L. U. Kelly, P. Moravek, J. Schubert, J. Wehnert

Journal:

International Urology and Nephrology

Year:

1986

Language:

english

File:

PDF, 559 KB

english, 1986

70

Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56a

F. H. Herrmann, K. Wulff, M. Schütz, M. Wehnert

Journal:

European Journal of Pediatrics

Year:

1990

Language:

english

File:

PDF, 379 KB

english, 1990

71

Die Meridionalgeschwindigkeit im Eintrittsgebiet eines Radialverdichters

Werner Wehnert, Hans Joachim Schröder

Journal:

Forschung im Ingenieurwesen

Year:

1968

Language:

german

File:

PDF, 479 KB

german, 1968

72

Die Hauptmann-Thannhauser-Muskeldystrophie und Differenzialdiagnosen von Myopathien mit Kontrakturen

F. Hanisch, S. Neudecker, M. Wehnert, S. Zierz

Journal:

Year:

2002

Language:

german

File:

PDF, 356 KB

german, 2002

73

Sympathisch unterhaltener Schmerz (SMP) – Phentolamintest vs. Sympathikusblockade

Y. Wehnert, B. Müller, B. Larsen, D. Kohn

Journal:

Year:

2002

Language:

german

File:

PDF, 296 KB

german, 2002

74

Serum levels of thrombopoietin, IL-11, and IL-6 in pediatric thrombocytopenias

M. Cremer, H. Schulze, G. Linthorst, C. C. Folman, S. Wehnert, G. Strauß, A. E. G. Kr. von dem Borne, K. Welte, M. Ballmaier

Journal:

Annals of Hematology

Year:

1999

Language:

english

File:

PDF, 92 KB

english, 1999

75

Determination of the genomic organization of human presenilin 1 by fiber-FISH analysis and restriction mapping of cloned DNA

Jessie Theuns, Marc Cruts, Jurgen Del-Favero, Dirk Goossens, Hans Dauwerse, Anita Wehnert, Johan T. den Dunnen, Christine Van Broeckhoven

Journal:

Mammalian Genome

Year:

1999

Language:

english

File:

PDF, 870 KB

english, 1999

76

Identification of mutational hot spots inLMNAencoding lamin A/C in patients with familial dilated cardiomyopathy

Andreas Perrot, Shwan Hussein, Volker Ruppert, Hartmut H. J. Schmidt, Manfred S. Wehnert, Nguyen Thuy Duong, Maximilian G. Posch, Anna Panek, Rainer Dietz, Ingrid Kindermann, Michael Böhm, Aleksandra

Journal:

Basic Research in Cardiology

Year:

2009

Language:

english

File:

PDF, 396 KB

english, 2009

77

Restrictive dermopathy: a rare laminopathy

Marc Thill, Thuy Duong Nguyen, Manfred Wehnert, Dorothea Fischer, Ingrid Hausser, Susanne Braun, Christian Jackisch

Journal:

Archives of Gynecology and Obstetrics

Year:

2008

Language:

english

File:

PDF, 455 KB

english, 2008

78

Restrictive dermopathy—a lethal congenital laminopathy. Case report and review of the literature

Paulo Morais, Sofia Magina, Maria do Céu Ribeiro, Manuela Rodrigues, José Manuel Lopes, Huong Le Thi Thanh, Manfred Wehnert, Hercília Guimarães

Journal:

European Journal of Pediatrics

Year:

2009

Language:

english

File:

PDF, 275 KB

english, 2009

79

Genomic structure and fine mapping of the two human filamin gene paraloguesFLNBandFLNCand comparative analysis of the filamin gene family

Christina Chakarova, Manfred S. Wehnert, Kerstin Uhl, Sadayappan Sakthivel, Hans-Peter Vosberg, Peter F. M. van der Ven, Dieter O. Fürst

Journal:

Year:

2000

Language:

english

File:

PDF, 2.15 MB

english, 2000

80

Identification, mapping, and genomic structure of a novel X-chromosomal human gene (SMPX) encoding a small muscular protein

D. Patzak, O. Zhuchenko, C.-C. Lee, M. Wehnert

Journal:

Year:

1999

Language:

english

File:

PDF, 216 KB

english, 1999

81

Mutations of theLMNAgene can mimic autosomal dominant proximal spinal muscular atrophy

Sabine Rudnik-Schöneborn, Elke Botzenhart, Thomas Eggermann, Jan Senderek, Benedikt G. H. Schoser, Rolf Schröder, Manfred Wehnert, Brunhilde Wirth, Klaus Zerres

Journal:

Year:

2007

Language:

english

File:

PDF, 284 KB

english, 2007

82

Emery-Dreifuss-Muskeldystrophie

Journal:

medizinische genetik

Year:

2009

Language:

german

File:

PDF, 403 KB

german, 2009

83

Reconstructions of the GaAs (1 1 3) surface

M. Pristovsek, H. Menhal, T. Wehnert, J.-T. Zettler, T. Schmidtling, N. Esser, W. Richter, C. Setzer, J. Platen, K. Jacobi

Journal:

Journal of Crystal Growth

Year:

1998

Language:

english

File:

PDF, 180 KB

english, 1998

84

Direct Transmission of a Hemoflagellate, Cryptobia salmositica (Kinetoplastida: Bodonina) Between Rainbow Trout Under Laboratory Conditions

PATRICK T. K. WOO, SYBILLE D. WEHNERT

Journal:

Journal of Eukaryotic Microbiology

Year:

1983

Language:

english

File:

PDF, 1.05 MB

english, 1983

85

Hereditary Neuralgic Amyotrophy: Mutation Analysis of Candidate Genes

J. MEULEMAN, G. KUHLENBÄUMER, A. SCHIRMACHER, M. WEHNERT, P. YOUNG, F. STÖGBAUER, E. B. RINGELSTEIN, C. VAN BROECKHOVEN, V. TIMMERMAN

Journal:

Annals of the New York Academy of Sciences

Year:

1999

File:

PDF, 184 KB

1999

86

Myofiber Degeneration in Autosomal Dominant Emery–Dreifuss Muscular Dystrophy (AD-EDMD) (LGMD1B)

Michel Mittelbronn, Frank Hanisch, Marc Gleichmann, Mechthild Stötter, Rudolf Korinthenberg, Manfred Wehnert, Gisèle Bonne, Sabine Rudnik-Schöneborn, Antje Bornemann

Journal:

Brain Pathology

Year:

2006

Language:

english

File:

PDF, 655 KB

english, 2006

87

Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families

Broeckhoven, C. Van, Genthe, A. M., Vandenberghe, A., Horsthemke, B., Backhovens, H., Raeymaekers, P., Hul, W. Van, Wehnert, A., Gheuens, J., Cras, P.

Journal:

Year:

1987

File:

PDF, 407 KB

1987

88

Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit-like repeats

Reiner, Orly, Carrozzo, Romeo, Shen, Ying, Wehnert, Manfred, Faustinella, Fabrizia, Dobyns, William B., Caskey, C. Thomas, Ledbetter, David H.

Journal:

Year:

1993

File:

PDF, 793 KB

1993

89

Apolipoprotein E4 allele in a population–based study of early–onset Alzheimer's disease

van Duijn, Cornelia M., de Knijff, Peter, Cruts, Marc, Wehnert, Anita, Havekes, Louis M., Hofman, Albert, Broeckhoven, Christine Van

Journal:

Nature Genetics

Year:

1994

File:

PDF, 513 KB

1994

90

Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample

Duijn, Cornelia M van, Cruts, Marc, Theuns, Jessie, Van Gassen, Geert, Backhovens, Hubert, van den Broeck, Marleen, Wehnert, Anita, Serneels, Sally, Hofman, Albert, Van Broeckhoven, Christine

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 183 KB

english, 1999

91

Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25

Meuleman, Jan, Kuhlenbäumer, Gregor, Schirmacher, Anja, Wehnert, Manfred, De Jonghe, Peter, De Vriendt, Els, Young, Peter, Airaksinen, Eila, Pou-Serradell, Adolfo, Prats, José-Maria

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 287 KB

english, 1999

92

Efficacy and safety of propiverine in SCI-patients suffering from detrusor hyperreflexia – A double-blind, placebo-controlled clinical trial

Stöhrer, M, Madersbacher, H, Richter, R, Wehnert, J, Dreikorn, K

Journal:

Year:

1999

Language:

english

File:

PDF, 158 KB

english, 1999

93

Eighteen novel mutations in patients with Lesch–Nyhan syndrome or partial hypoxanthine phosphoribosyltransferase deficiency

I. Willers, H. Bolz, M. Wehnert, A. Gal

Journal:

Journal of Inherited Metabolic Disease

Year:

1999

Language:

english

File:

PDF, 34 KB

english, 1999

94

Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chain

I. Wittig, P. Augstein, G. K. Brown, T. Fujii, A. Rötig, P. Rustin, A. Munnich, P. Seibel, D. Thorburn, B. Wissinger, K. Tamboom, A. Metspalu, E. Lamantea, M. Zeviani, M. S. Wehnert

Journal:

Journal of Inherited Metabolic Disease

Year:

2001

Language:

english

File:

PDF, 126 KB

english, 2001

95

Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybrids

Guy Van Camp, Wim Van Hul, Hubert Backhovens, Piet Stinissen, Anita Wehnert, David Patterson, Antoon Vandenberghe, Christine Van Broeckhoven

Journal:

Somatic Cell and Molecular Genetics

Year:

1990

Language:

english

File:

PDF, 843 KB

english, 1990

96

A more efficient waveform for cardiac stimulation

O. Z. Roy, R. W. Wehnert

Journal:

Medical and Biological Engineering and Computing

Year:

1971

Language:

english

File:

PDF, 399 KB

english, 1971

97

A simple linear pulse-to-pulse cardiac tachometer

O. Z. Roy, R. W. Wehnert

Journal:

Medical and Biological Engineering and Computing

Year:

1974

Language:

english

File:

PDF, 172 KB

english, 1974

98

Improvements in biogalvanic energy sources

O. Z. Roy, R. W. Wehnert

Journal:

Medical and Biological Engineering and Computing

Year:

1974

Language:

english

File:

PDF, 432 KB

english, 1974

99

Klimawandel und mehr: aktuelle Themen in „Raumforschung und Raumordnung“

Dr. Andreas Klee, Johannes Schulte, Hendrikje Wehnert

Journal:

Raumforschung und Raumordnung

Year:

2012

Language:

german

File:

PDF, 523 KB

german, 2012

100

Die Komplexität der (Kultur-)Landschaft

Hendrikje Wehnert

Journal:

Raumforschung und Raumordnung

Year:

2012

Language:

german

File:

PDF, 124 KB

german, 2012