Andre Reis - Dissemin

Papers authored by Andre Reis

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1998 M. Raghunath, Hans Christian Hennies, Florian Velten, Victor Wiebe, Peter M. Steinert, Andre Reis

, Heiko Traupe

A novel in situ method for the detection of deficient transglutaminase activity in the skin

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Kathrin Saar, Detlev Schindler, Rolf-Dieter Wegner, André Reis

, Thomas F. Wienker, Holger Hoehn, Hans Joenje, Karl Sperling, Martin Digweed

Localisation of a Fanconi anaemia gene to chromosome 9p

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Karin Buiting, Barbel Dittrich, Stephanie Gross, Christina Lich, Claudia Farber, Claudia Färber, Tina Buchholz, Ellie Smith, Andre Reis

, Joachim Bürger, Markus M. Nöthen, Ulli Barth-Witte, Bart Janssen, Dvorah Abeliovich, Israela Lerer and 21 other authors

Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.

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Hans Christian Hennies, Wolfgang Küster, Victor Wiebe, Alice Krebsová, André Reis

Genotype/phenotype correlation in autosomal recessive lamellar ichthyosis.

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Raymonda Varon, Christine Vissinga, Matthias Platzer, Karen M. Cerosaletti, Krystyna H. Chrzanowska, Kathrin Saar, Georg Beckmann, Eva Seemanová, Paul R. Cooper, Norma J. Nowak, Markus Stumm, Corry M. R. Weemaes, Richard A. Gatti, Richard K. Wilson, Martin Digweed and 4 other authors

Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

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John Mulley, Kathrin Saar, Gerry Hewitt, Franz Rüschendorf, Hilary Phillips, Alison Colley, David Sillence, André Reis

, Meredith Wilson

Gene localization for an autosomal dominant familial periodic fever to 12p13.

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Hans Christian Hennies, Michael Raghunath, Victor Wiebe, Melanie Vogel, Florian Velten, Heiko Traupe, André Reis

Genetic and immunohistochemical detection of mutations inactivating the keratinocyte transglutaminase in patients with lamellar ichthyosis

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Rh Wallace, Dw Wang, R. Singh, Ie Scheffer, Al George, Ha Phillips, K. Saar, A. Reis

, Ew Johnson, Gr Sutherland, Sf Berkovic, Jc Mulley

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta 1 subunit gene SCN1B

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C. Thies, K. Sperling, A. Reis

, M. Handrock

Small malformations of the middle ear - a hereditary defect?

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1997 Martin Walter Laass, Hans Christian Hennies, Sabine Preis, Howard P. Stevens, Martin Jung, Irene M. Leigh, Thomas F. Wienker, André Reis

Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping

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Peter Nürnberg, Sigrid Tinschert, Michal Mrug, Jochen Hampe, Clemens R. Müller, Eike Fuhrmann, Hans-Steffen Braun, André Reis

The gene for autosomal dominant craniometaphyseal dysplasia maps to chromosome 5p and is distinct from the growth hormone-receptor gene.

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Michelle Starfield, Hans Christian Hennies, Martin Jung, Trefor Jenkins, Thomas Wienker, Peter Hull, Amanda Spurdle, Wolfgang Küster, Michele Ramsay, André Reis

Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakers.

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Joachim Bürger, Karin Buiting, Bärbel Dittrich, Stephanie Gross, Christina Lich, Karl Sperling, Bernhard Horsthemke, André Reis

Different mechanisms and recurrence risks of imprinting defects in Angelman syndrome.

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K. Saar, Kh H. Chrzanowska, M. Stumm, M. Jung, G. Nürnberg, Tf F. Wienker, E. Seemanová, Rd D. Wegner, A. Reis

, K. Sperling

The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21.

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M. Macek, A. Krebsova, E. Nash, A. Hamosh, A. Reis

, R. Varonmateeva, J. Schmidtke, Ne Maestri, K. Sperling, M. Krawczak, Gr Cutting

Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survival

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Rachel L. Robinson, Nicole Monnier, Werner Wolz, Martin Jung, André Reis

, Gudrun Nuernberg, Julie L. Curran, Koen Monsieurs, Paul Stieglitz, Luc Heytens, Ruth Fricker, Christine van Broeckhoven, Van Christine Broeckhoven, Thomas Deufel

, Phil M. Hopkins and 2 other authors

A genome wide search for susceptibility loci in three European malignant hyperthermia pedigrees

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1996 Joachim Bürger, Jürgen Kunze, Karl Sperling, André Reis

Phenotypic differences in Angelman syndrome patients: Imprinting mutations show less frequently microcephaly and hypopigmentation than deletions

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Joachim Bürger, Hermann Metzke, Caroline Paternotte, Frank Schilling, Jamilé Hazan, André Reis

Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family

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Micha&lstrok; Witt, Andre Reis

, Wojciech Cichy, Katarzyna Dziechciowska

Microsatellite Haplotypes of Polish Cystic Fibrosis Alleles: ΔF508 Chromosomes Demonstrate a North-South Haplotype Frequency Gradient

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G. Linss, E. Gebel, A. Reis

, R. D. Wegner, D. Prutz

Localisation of the gene for the naevoid basal cell carcinoma syndrome (Gorlin-Goltz syndrome) and other cytological investigations in one family

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Papers authored by Andre Reis