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المؤلفون: Bernhard, Steiner, Jonas, Rosendahl, Heiko, Witt, Niels, Teich, Volker, Keim, Hans-Ulrich, Schulz, Roland, Pfützer, Matthias, Löhr, Matthias, Lühr, Thomas M, Gress, Renate, Nickel, Olfert, Landt, Monika, Koudova, Milan, Macek, Antoni, Farre, Teresa, Casals, Marie-Claire, Desax, Sabina, Gallati, Macarena, Gomez-Lira, Marie Pierre, Audrezet, Claude, Férec, Marie, des Georges, Mireille, Claustres, Kaspar, Truninger
المساهمون: Institute of Medical Microbiology [Zurich], Universität Zürich [Zürich] = University of Zurich (UZH), Etablissement Français du Sang Bretagne, EFS, Department of Gastroenterology, University of Marburg, Department of Biology and Medical Genetics, Charles University Prague, Medical School and University, The Weatherall Institute of Molecular Medicine, University of Oxford [Oxford], Génétique, génomique fonctionnelle et biotechnologies (UMR 1078) (GGB), Institut Brestois Santé Agro Matière (IBSAM), Université de Brest (UBO)-Université de Brest (UBO)-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire de génétique des maladies rares. Pathologie moleculaire, etudes fonctionnelles et banque de données génétiques (LGMR), IFR3, Université Montpellier 1 (UM1)-Université Montpellier 1 (UM1)-Université de Montpellier (UM)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), University of Zurich, Truninger, K
المصدر: Human Mutation
Human Mutation, Wiley, 2011, 32 (8), pp.912-920. ⟨10.1002/humu.21511⟩
HUMAN MUTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instnameمصطلحات موضوعية: Male, 10039 Institute of Medical Genetics, [SDV]Life Sciences [q-bio], Cystic Fibrosis Transmembrane Conductance Regulator, medicine.disease_cause, Gastroenterology, Vas Deferens, Male Urogenital Diseases, Genotype, Genetics(clinical), CFTR, Child, Genetics (clinical), Genetics, 0303 health sciences, Mutation, education.field_of_study, integumentary system, musculoskeletal, neural, and ocular physiology, 030305 genetics & heredity, Vas deferens, Middle Aged, 3. Good health, idiopathic chronic pancreatitis, medicine.anatomical_structure, Trypsin Inhibitor, Kazal Pancreatic, CBAVD, Adult, 2716 Genetics (clinical), medicine.medical_specialty, Adolescent, Genetic counseling, Population, 610 Medicine & health, Biology, Young Adult, 03 medical and health sciences, 1311 Genetics, Pancreatitis, Chronic, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, education, Infertility, Male, 030304 developmental biology, Haplotype, Epistasis, Genetic, Heterozygote advantage, medicine.disease, nervous system diseases, Haplotypes, 570 Life sciences, biology, Pancreatitis, Carrier Proteins
وصف الملف: Steiner_et_al,_Common_CFTR_haplotypes.pdf - application/pdf