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1دورية أكاديمية
المصدر: Atherosclerosis Plus, Vol 57, Iss , Pp 26-29 (2024)
مصطلحات موضوعية: Island of Nias, Genetic bottleneck, Hyperglycemia, Hyperlipidemia, Diseases of the circulatory (Cardiovascular) system, RC666-701
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Alexa Haeger, Christophe Pouzat, Volker Luecken, Karim N’Diaye, Christian Elger, Ingo Kennerknecht, Nikolai Axmacher, Vera Dinkelacker
المصدر: Frontiers in Behavioral Neuroscience, Vol 15 (2021)
مصطلحات موضوعية: prosopagnosia, fusiform face area (FFA), perception, representational similarity analysis (RSA), Donsker’s random walk analysis, working memory, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Uschi Lindert, Wayne A. Cabral, Surasawadee Ausavarat, Siraprapa Tongkobpetch, Katja Ludin, Aileen M. Barnes, Patra Yeetong, Maryann Weis, Birgit Krabichler, Chalurmpon Srichomthong, Elena N. Makareeva, Andreas R. Janecke, Sergey Leikin, Benno Röthlisberger, Marianne Rohrbach, Ingo Kennerknecht, David R. Eyre, Kanya Suphapeetiporn, Cecilia Giunta, Joan C. Marini, Vorasuk Shotelersuk
المصدر: Nature Communications, Vol 7, Iss 1, Pp 1-12 (2016)
مصطلحات موضوعية: Science
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2041-1723
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4دورية أكاديمية
المصدر: Case Reports in Genetics, Vol 2017 (2017)
وصف الملف: electronic resource
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5دورية أكاديمية
المصدر: i-Perception, Vol 7 (2016)
مصطلحات موضوعية: Psychology, BF1-990
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2041-6695
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6دورية أكاديمية
المؤلفون: Rainer Stollhoff, Jürgen Jost, Tobias Elze, Ingo Kennerknecht
المصدر: PLoS ONE, Vol 6, Iss 1, p e15702 (2011)
وصف الملف: electronic resource
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7دورية أكاديمية
المؤلفون: Rainer Stollhoff, Jürgen Jost, Tobias Elze, Ingo Kennerknecht
المصدر: PLoS ONE, Vol 5, Iss 7, p e11482 (2010)
وصف الملف: electronic resource
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8
المؤلفون: Nathalie Escande-Beillard, Ingo Kennerknecht, Umut Altunoglu, Katta M. Girisha, Shalini S. Nayak, Hülya Azaklı, Anju Shukla, Susanne Ledig, Esra Börklü, Serpil Eraslan, Hülya Kayserili
المصدر: Clinical geneticsREFERENCES. 101(2)
مصطلحات موضوعية: Infertility, Male, Secondary sex characteristic, Disorders of Sex Development, Gonadal dysgenesis, XX gonadal dysgenesis, Biology, Polymorphism, Single Nucleotide, Germline, XY gonadal dysgenesis, Consanguinity, Hypergonadotropic hypogonadism, Genetics, medicine, Humans, Sex organ, Abnormalities, Multiple, Genetic Predisposition to Disease, Protein Phosphatase 2, Genetics (clinical), Genetic Association Studies, Gonadal Dysgenesis, 46,XY, Facies, medicine.disease, Gonadal Dysgenesis, 46,XX, Pedigree, Phenotype, Mutation, Female
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المؤلفون: Shalini S. Nayak, Serpil Eraslan, Hülya Kayserili, Ingo Kennerknecht, Hülya Azaklı, Nathalie Escande-Beillard, Susanne Ledig, Esra Börklü, Katta M. Girisha, Anju Shukla, Umut Altunoglu
مصطلحات موضوعية: medicine.medical_specialty, Endocrinology, Internal medicine, medicine, XX gonadal dysgenesis, Biology, medicine.disease, XY gonadal dysgenesis
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::29dea6d022b10d68d65e7e368660d25f
https://doi.org/10.1111/cge.14086/v2/response1 -
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المؤلفون: Arif O. Khan, Susanne Markus, Raoul Heller, Solaf M. Elsayed, Ute Steinhauer, Heike M. Korbmacher, Kerstin Nagel-Wolfrum, Markus Pfister, Diana Mitter, Christian Decker, Birgit Lorenz, Markus N. Preising, Ingo Kennerknecht, Shahid Mahmood Baig, Heidi Stöhr, Cornelie Müller-Hofstede, Klaus Rohrschneider, Fabian Moeller, Peter Charbel Issa, Tobias Eisenberger, Christine Neuhaus, Hanno J. Bolz, Klaus Rüther, Sandra Nagl, Bodo B. Beck, Cornelia Blank, Dagmar Huhle, Hesham Taha
المصدر: Molecular Genetics & Genomic Medicine
مصطلحات موضوعية: 0301 basic medicine, Usher syndrome, Nonsense mutation, next‐generation sequencing, Biology, Gene mutation, Bioinformatics, 03 medical and health sciences, symbols.namesake, Retinitis pigmentosa, Genetics, medicine, otorhinolaryngologic diseases, Multiplex ligation-dependent probe amplification, Nonsyndromic deafness, Molecular Biology, Genetics (clinical), Sanger sequencing, Heimler syndrome, Copy number variation, Point mutation, Original Articles, medicine.disease, eye diseases, 030104 developmental biology, symbols, phenocopies, translational read‐through, Original Article