Resultados de procura - Steffan Loff
- Mostrando 1 - 4 Resultados de 4
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High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome por Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, Steffan Loff, Walter Back, Constanze Pagenstecher, D. Ross McLeod, Gail E. Graham, Elisabeth Mangold, René Santer, Peter Propping, Waltraut Friedl
Publicado 2005Artigo -
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High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome por Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, M. Stolte, Mark M. Entius, Steffan Loff, Walter Back, Astrid Kaufmann, KM Keller, Stefan Blaas, Reiner Siebert, Stefanie Vogt, S Spranger, Elke Holinski‐Feder, Lone Sunde, Peter Propping, W Friedl
Publicado 2007Artigo -
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Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3. por Sylviane Olschwang, David Markie, S. Seal, Kay Neale, Rita J. S. Phillips, S Cottrell, Ian O. Ellis, Shirley Hodgson, Peter Zauber, AD Spigelman, Takeo Iwama∥, Steffan Loff, C. McKeown, Cristiana Marchese, Jeffrey R. Sampson, Sally Davies, I C Talbot, J A Wyke, Gilles Thomas, Walter F. Bodmer, Akseli Hemminki, Egle Avizienyte, Albert de la Chapelle, Lauri A. Aaltonen, Ian Tomlinson
Publicado 1998Artigo
Ferramentas de procura:
Materias Relacionadas
Biology
Gene
Genetics
Exon
Germline mutation
Multiplex ligation-dependent probe amplification
Mutation
Point mutation
Allele
Cancer research
Frameshift mutation
Genetic linkage
Genotype
Genotype-phenotype distinction
KRAS
Locus (genetics)
Medicine
Molecular biology
Mutation testing
Pathology
Peutz–Jeghers syndrome
Phenotype
STK11