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Browsing by Author "Bernd Wollnik"DSpace@Sakarya
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Browsing by Author "Bernd Wollnik" ... DNA double-strand breaks (DSBs) are highly toxic lesions, which, if not properly repaired, can give rise to genomic ... Browsing by Author "Bernd Wollnik" ... DNA double-strand breaks (DSBs) are highly toxic lesions, which, if not properly repaired, can give rise to genomic ...
Activating Somatic FGFR2 Mutations in Breast Cancer - PLOSjournals.plos.org › plosone › article › authors › jour...
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· Nadine Reintjes, · Yun Li, · Alexandra Becker, · Edyta Rohmann, · Rita Schmutzler, · Bernd Wollnik.
About the AuthorsPLOS
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— Bernd Wollnik. Affiliations Institute of Human Genetics, University Hospital of Cologne, Cologne, Germany, Center for Molecular Medicine ... › article
Epstein's Inborn Errors of Development: The Molecular Basis ...google.no
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... BERND WOLLNIk Institute of Human Genetics, University of Goettingen, Goettingen, Germany and Institute of Human Genetics, University of Cologne, Cologne ...
Mutations in Human Genetic Diseasegoogle.no
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... Bernd Wollnik, and Joseph Schlessinger. Structural basis for reduced fgfr2 activity in ladd syndrome: Implications for fgfr autoinhibition and activation ...
Rare Diseases: Integrative PPPM Approach as the Medicine of ...google.no
books.google.no
... Bernd Wollnik Abstract Rare diseases are a heavy burden on affected individuals and, collectively, on society. Since most rare diseases have a genetic cause ...
Einladung zum Syndromtag in Göttingen vom 04.De Gruyter
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von B Wollnik — ... Bernd Wollnik. Tagungsleitung. Prof. Dr. med. Bernd Wollnik. Prof. Dr. rer. nat. Uwe Kornak. Universitätsmedizin Göttingen. Institut für ... von B Wollnik — ... Bernd Wollnik. Tagungsleitung. Prof. Dr. med. Bernd Wollnik. Prof. Dr. rer. nat. Uwe Kornak. Universitätsmedizin Göttingen. Institut für ...
Medizinische Genetik Volume 27 Issue 4De Gruyter
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Molekulare Grundlagen der autosomal-rezessiven primären Mikrozephalie. Gökhan Yigit, Nadine Rosin, Bernd Wollnik. Page range: ; Kopfumfang bei Kindern ... Molekulare Grundlagen der autosomal-rezessiven primären Mikrozephalie. Gökhan Yigit, Nadine Rosin, Bernd Wollnik. Page range: ; Kopfumfang bei Kindern ...
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Increasing the Yield in Targeted Next-Generation Sequencing by ...journals.plos.org › plosone › article › authors › jour...
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· Bernd Wollnik. Affiliations Institute of Human Genetics, University Hospital of Cologne, Cologne, Germany, Center for Molecular Medicine ...
Epstein's Inborn Errors of Development: The Molecular Basis ...google.al
books.google.al
... MD Research Professor Facharzt für Pädiatrie und Humangenetik JOHAN P. DE WINTER BERND WOLLNIk Institute of Human Genetics, University of Goettingen, ...
Mutations in Human Genetic Diseasegoogle.al
books.google.al
[31] Erin D Lew, Jae Hyun Bae, Edyta Rohmann, Bernd Wollnik, and Joseph Schlessinger. Structural basis for reduced fgfr2 activity in ladd syndrome: ...
Rare Diseases: Integrative PPPM Approach as the Medicine of ...google.al
books.google.al
in Rare Diseases Filippo Beleggia and Bernd Wollnik Abstract Rare diseases are a heavy burden on affected individuals and, collectively, on society.
Epstein's Inborn Errors of Development: The Molecular Basis of...
books.google.de
This third edition of Epstein's Inborn Errors of Development provides essays on pathways of development and thoughtful reviews of dysmorphic syndromes for...
Mutations in Human Genetic Disease - Google Books
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Different types of mutation can vary in size, from structural variants to single base-pair substitutions, but what they all have in common is that their...
Verwandte Suchanfragen zu Bernd Wollnik
| Dagmar Wieczorek Holger Arndt Stavros Kangarakis | Adil Arrouj Stephanie Jung Meliha Karsak | Gamze Güven Peter Milena Czarnecki |
Personen Vorname "Bernd" (49284) Name "Wollnik" (179) |
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