-
1
المؤلفون: Elisabeth Mangold, Peter Tessmann, Rocio Ortiz-Lopez, Heiko Reutter, Markus M. Nöthen, Anne C. Böhmer, Stefanie Nowak, Philipp Wahle, Kerstin U. Ludwig, Augusto Rojas-Martinez, Mario Paredes-Zenteno, Sergio G. Munoz-Jimenez, Michael Knapp
المصدر: Birth Defects Research Part A: Clinical and Molecular Teratology. 100:43-47
مصطلحات موضوعية: Genetics, Embryology, education.field_of_study, Population, Case-control study, Single-nucleotide polymorphism, General Medicine, Biology, Polymorphism (computer science), Pediatrics, Perinatology and Child Health, Genetic predisposition, IRF6, Allele, education, Developmental Biology, Genetic association
-
2
المؤلفون: Khalid Aldhorae, Franz-Josef Kramer, Hannah Schuenke, Gül Schmidt, Elisabeth Mangold, Johanna Klamt, Janis Stavusis, Heiko Reutter, Rudolf Reiter, Pinar Gültepe, Guntram Borck, Markus M. Nöthen, Andrea Hofmann, Miho Ishida, Bert Braumann, Ruth Raff, Philip Stanier, Nina Ishorst, Baiba Lace, Anne C. Böhmer, Michael Knapp, Alexander Hemprich, Sibylle Brosch, Lina Gölz, Gudrun E. Moore, Ann-Kathrin Hoebel, Peter Tessmann, Rimante Seselgyte, Stefanie Nowak, Kerstin U. Ludwig, Andreas Jäger, Rudolf H. Reich, Thomas Kreusch
المصدر: American journal of human genetics. 98(4)
مصطلحات موضوعية: 0301 basic medicine, Genetic counseling, Cleft Lip, Genome-wide association study, 030105 genetics & heredity, Biology, medicine.disease_cause, Polymorphism, Single Nucleotide, 03 medical and health sciences, Open Reading Frames, Polymorphism (computer science), Report, medicine, Genetics, Coding region, Humans, Van der Woude syndrome, Genetics(clinical), Abnormalities, Multiple, Genetic Predisposition to Disease, Allele, Genetics (clinical), Alleles, Mutation, Cysts, Racial Groups, medicine.disease, Lip, Minor allele frequency, Cleft Palate, DNA-Binding Proteins, 030104 developmental biology, Case-Control Studies, Transcription Factors
-
3
المؤلفون: Kerstin U, Ludwig, Philipp, Wahle, Heiko, Reutter, Mario, Paredes-Zenteno, Sergio G, Muñoz-Jimenez, Rocio, Ortiz-Lopez, Anne C, Böhmer, Peter, Tessmann, Stefanie, Nowak, Markus M, Nöthen, Michael, Knapp, Augusto, Rojas-Martinez, Elisabeth, Mangold
المصدر: Birth defects research. Part A, Clinical and molecular teratology. 100(1)
مصطلحات موضوعية: Genetic Markers, Male, Risk, Genotyping Techniques, Models, Genetic, Cleft Lip, Indians, South American, Inheritance Patterns, Polymorphism, Single Nucleotide, Mass Spectrometry, Cleft Palate, Gene Frequency, Genetic Loci, Case-Control Studies, Humans, Female, Genetic Predisposition to Disease, Mexico, Alleles, Polymorphism, Restriction Fragment Length, Genome-Wide Association Study
-
4
المؤلفون: K. Dobson, Silke Redler, Pattie Birch, Kathrin A. Giehl, Hans Wolff, Peter Teßmann, Dmitriy Drichel, Markus M. Nöthen, Regina C. Betz, Rachid Tazi-Ahnini, Sandra Hanneken, Andrew G. Messenger, Ulrike Blume-Peytavi, Markus Böhm, Hassnaa Mahmoudi, Tim Becker, Gerhard Lutz, Roland Kruse
المصدر: Archives of dermatological research 305(3), 249-253 (2012). doi:10.1007/s00403-012-1296-3
مصطلحات موضوعية: medicine.medical_specialty, Genotype, Dermatology, Biology, Hypotrichosis, Polymorphism, Single Nucleotide, genetics [Obesity], Internal medicine, Diabetes mellitus, medicine, Humans, Genetic Predisposition to Disease, Obesity, ddc:610, Genetic Association Studies, genetics [Hypotrichosis], Case-control study, Genetic Variation, General Medicine, Hair follicle, medicine.disease, Melanocortin 4 receptor, genetics [Receptor, Melanocortin, Type 4], medicine.anatomical_structure, Endocrinology, Hair loss, Case-Control Studies, Receptor, Melanocortin, Type 4, Male-pattern baldness, Female, MC4R protein, human, Hormone
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5e0299d7eec0b1fa4e907557f97db48
https://pub.dzne.de/record/136859 -
5
المؤلفون: Paola Franceschelli, Marieke Bouwman-Both, Peter A. Mossey, Régine P.M. Steegers-Theunissen, Kerstin U. Ludwig, Markus M. Nöthen, Peter Tessmann, Jan Lindemans, Anne C. Böhmer, Anne M. Molloy, Elisabeth Mangold, Borut Peterlin, V. Aiello, Michael Knapp, Michele Rubini
المساهمون: Obstetrics & Gynecology, Clinical Chemistry
المصدر: American Journal of Medical Genetics. Part A, 161, 2545-2549
American Journal of Medical Genetics. Part A, 161, 10, pp. 2545-2549
American Journal of Medical Genetics Part A, 161(10), 2545-2549. Wiley-Liss Inc.مصطلحات موضوعية: Risk, Genotype, Cleft Lip, Population, Quantitative Trait Loci, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, White People, Palatoschisi, Genetics, Genetica medica, SNP, Humans, Genetic Predisposition to Disease, Craniofacial, education, Gene, Labiopalatoschisi, Genetics (clinical), Alleles, Genetic Association Studies, Genetic association, education.field_of_study, Phenotype, Cleft Palate, Human Reproduction [NCEBP 12], Etiology
وصف الملف: application/pdf
-
6
المؤلفون: Silke Redler, Felix F. Brockschmidt, Stefanie Heilmann, Hans Wolff, Markus M. Nöthen, Gerhard Lutz, Kathrin A. Giehl, Roland Kruse, Sabrina Wolf, Ulrike Blume-Peytavi, Natalie Garcia Bartels, K. Dobson, Peter Teßmann, Pattie Birch, Dmitriy Drichel, Markus Böhm, Andrew G. Messenger, Regina C. Betz, Rachid Tazi-Ahnini, Sandra Hanneken, Tim Becker
المصدر: Journal of dermatological science 72(2), 186-188 (2013). doi:10.1016/j.jdermsci.2013.06.012
مصطلحات موضوعية: pathology [Hair], Male, ultrastructure [Chromosomes], Genotype, Dermatology, Biochemistry, Polymorphism, Single Nucleotide, Chromosomes, Polymorphism (computer science), Germany, Medicine, Humans, Genetic Predisposition to Disease, ddc:610, Allele, Molecular Biology, Alleles, genetics [Alopecia], Oligonucleotide Array Sequence Analysis, Genetics, business.industry, Haplotype, Case-control study, Alopecia, medicine.disease, United Kingdom, Matrix-assisted laser desorption/ionization, Hair loss, Haplotypes, Case-Control Studies, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Susceptibility locus, Female, business, Hair
-
7
المؤلفون: Martin Hautzinger, Manuel Mattheisen, Srdjan Djurovic, Jennifer Vollmer, Marian L. Hamshere, Michael Alexander, Alexander S. Tiganov, Maria Grigoroiu-Serbanescu, Johanna Sasse, Markus J. Schwarz, Scott D. Gordon, Michael Bauer, Lilia I. Abramova, René Breuer, H.-Erich Wichmann, Susanne Lucae, Susanne Moebus, Britta Haenisch, Carmen C. Diaconu, Grant W. Montgomery, Johannes Schumacher, Kari Stefansson, Jean-Pierre Kahn, Nicholas G. Martin, Wolfgang Maier, Piotr M. Czerski, Michael Steffens, Frank Bellivier, Ole A. Andreassen, Mark Lathrop, Joanna Hauser, Bertram Müller-Myhsok, Stéphane Jamain, Thomas F. Wienker, Omar Gustafsson, Hreinn Stefansson, Nicholas John Craddock, Lejla Kapur-Pojskić, Peter Tessmann, Chantal Henry, Fermín Mayoral, Michael Conlon O'Donovan, Jutta Kammerer-Ciernioch, Fabio Rivas, Liliana Oruc, Markus M. Nöthen, Alexander Chuchalin, Andreas Zimmer, Moritz Weingarten, Stefan Schreiber, Engilbert Sigurdsson, Sven Cichon, Adam Wright, Bruno Etain, Marcella Rietschel, Peter Propping, Franziska Degenhardt, Simon Heath, Thomas G. Schulze, Christine Schmäl, Galina Pantelejeva, Michael John Owen, Helmut Vedder, Christian Meesters, Andreas Reif, Gulja Babadjanova, Philip B. Mitchell, Jana Strohmaier, Thomas W. Mühleisen, Peter R. Schofield, Stefan Herms, Marion Leboyer, Stacy Steinberg, Sarah E. Medland, Lutz Priebe, Xavier Miró
المصدر: The American Journal of Human Genetics. (3):372-381
مصطلحات موضوعية: Postmortem studies, Bipolar Disorder, Medizin, Genome-wide association study, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Mice, 0302 clinical medicine, Neurocan, Report, medicine, Genetics, Animals, Humans, Genetics(clinical), Genetic Predisposition to Disease, Bipolar disorder, Genetics (clinical), 030304 developmental biology, 0303 health sciences, Haplotype, Case-control study, Brain, Genetic Variation, Reproducibility of Results, Odds ratio, medicine.disease, 3. Good health, Case-Control Studies, 030217 neurology & neurosurgery, Follow-Up Studies, Genome-Wide Association Study
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8372750100a2d11d32ccfa1515e67abf
Full Text via ClinicalKey