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wienervideo&filmtage
archiv.videoundfilmtage.at
Bildein von Eva Hausberger und Gerhard Daurer. being u.m.f. von Johannes Breit. Die Leiden des Action Werther von Bernt Popp und Birgit ...
Netzwerk-Profile
OPUS FAU | Suchen
opus4.kobv.de
Bernt Popp (1) Cheol-Sang Hwang (1) Dagmar Wieczorek (1) Eva-Christina Prott (1) + more. Year of publication (2) (1) (1) Keywords - (4) Attention (1)
Firmen-Mitarbeiter
GfH - Ehrungen
gfhev.de
Helmholtz Zentrum München, für ihre Dissertation "Discovery and validation of ... Bernt Popp, Humangenetische Institut der Friedrich-Alexander-Universität ...
Bücher
HEIDI: Freunscht, Inga: Behavioral phenotype in five individuals with...
katalog.ub.uni-heidelberg.de
Verf.angabe: Inga Freunscht, Bernt Popp, Rainer Blank, Sabine Endele, Ute Moog, Holger Petri, Eva-Christina Prott, Andre Reis, Jochen Rübo, Bernhard Zabel, ...
Advanced Search | American Society of Nephrology
jasn.asnjournals.org
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OPUS FAU | Medizinische Fakultät -ohne weitere Spezifikation-
opus4.kobv.de
Bernt Popp (1) Bertold Renner (1) Bettina Hofmiller (1) Bettina Plank-Kiegele (1) Bettina Rau (1) Bettina Schwamb (1) Betty van der Veen (1) Biancamaria Beck (1)
Dokumente zum Namen
[ ] High-speed and accurate color-space short-read alignment...
arxiv.org
High-speed and accurate color-space short-read alignment with CUSHAW2. Yongchao Liu, Bernt Popp, Bertil Schmidt. Summary: We present ...
Quantitative Biology authors/titles (555 skipped)
arxiv.org
Authors: Yongchao Liu, Bernt Popp, Bertil Schmidt. Comments: 2 pages,1 table. Subjects: Genomics (q-bio.GN). [571] arXiv: [pdf, other]. Title: The ...
Wissenschaftliche Veröffentlichungen
DFG - GEPRIS - Dr. Bernt Poppgepris.dfg.de › gepris › person
gepris.dfg.de
Dr. Bernt Popp, Institut für HumangenetikLeipzig.
Es fehlt: München" | Muss Folgendes enthalten: München"
Behavioral phenotype in five individuals with de novo ...behavioralandbrainfunctions.biomedcentral.com › ...
behavioralandbrainfunctions.biomedcentral.com
1994, München: Deutsche Akademie für Entwicklungsrehabilitation, Bernt Popp, Sabine Endele, Andre Reis & Martin Zenker. Klinik für ...
Bernt Popp – ScienceOpen
www.scienceopen.com
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Authors: Yorck ...
Personenindex - DFG - GEPRISgepris.dfg.de › gepris › OCTOPUS
gepris.dfg.de
Popov, Tzvetan, München. Popov, Tzvetan, Mannheim ... Popp, Alexander, Neubiberg. Popp, Andreas, Berlin. Popp, Bernt, Leipzig. Popp, Dietmar, Marburg.
Veröffentlichungen allgemein
Behavioral phenotype in five individuals with de novo mutations...
link.springer.com
(1); Bernt Popp · (2); Rainer Blank · (3); Sabine Endele · ...
Oalib search
www.oalib.com
Abstract: The majority of next-generation sequencing short-reads can be properly aligned by leading aligners at high speed. However, the alignment quality can ...
Sonstiges
外文检索-中国知网
scholar.cnki.net
CNKI学术搜索是一个基于海量资源的跨学科、跨语种、跨文献类型的学术资源搜索平台，其资源库涵盖各类学术期刊、论文、报纸、专利、标准、年鉴、工具书等，旨在为国内外研究人员提供全面、权威、系统的知识网络。
Epilepsy: Popp, Bernt - Expertscape.com
www.expertscape.com
Bernt Popp has special expertise in Epilepsy
OPUS FAU | Behavioral phenotype in five individuals with de novo...
opus4.kobv.de
Metadaten; Author: Inga Freunscht, Bernt Popp, Rainer Blank, Sabine Endele, Ute Moog, Holger Petri, Eva-Christina Prott, Andre Reis, Jochen Rübo, Bernhard Zabel ...
Klinische Genomik - Universitätsklinikum Leipzigwww.uniklinikum-leipzig.de › genetische-diagnostik
www.uniklinikum-leipzig.de
Während ihrer Promotion an der LMU in München beschäftigte sie sich mit ... Bernt Popp studierte Humanmedizin und promovierte zum Thema der ...
Kunstmann, Heinrich - KIT-Bibliothek: Karlsruher Virtueller ...kvk.bibliothek.kit.edu › hylib-bin › kvk › nph-kvk2 › fo...
kvk.bibliothek.kit.edu
... stature / by Nadine N. Hauer, Bernt Popp, Leila Taher, Carina Vogl, Perundurai S. Dhandapany, Christian Büttner, Steffen Uebe, Heinrich Sticht, Fulvia …
"Expanding the Phenotype Associated with NAA10-Related N-Terminal...
hsrc.himmelfarb.gwu.edu
Bernt Popp · Bénédicte Gérard · Marina Blenski · Nicholas AhMew, George Washington University · +several additional authors ...
All variants in the NAA10 gene - Global Variome shared LOVD
databases.lovd.nl
PubMed: Rope et al , {DOI:Rope et al :doi: j.ajhg }, OMIM:var0001, -, rs , Germline, yes, -, -, 0, -, Bernt Popp.
CUSHAW3: Sensitive and Accurate Base-Space and Color-Space Short-Read...
journals.plos.org
The majority of next-generation sequencing short-reads can be properly aligned by leading aligners at high speed. However, the alignment quality can still be...
All transcript variants in gene NAA10 - Global Variome shared LOVD
databases.lovd.nl
Curator: Bernt Popp · NAA10 homepage · View transcripts · View variants · View individuals · View diseases · View screenings · Submit new data · LOVD ...
Altmetric – Is MED13L-related intellectual disability a recognizable...
sdu.altmetric.com
... Maria Kibæk, Lone Laulund, Niels Illum, Ulrike Dunkhase-Heinl, Antje Wiesener, Bernt Popp, Giuseppe Marangi, Tina Duelund Hjortshøj, Jakob Ek, Ida Vogel, ...
OPUS FAU | CUSHAW3: Sensitive and Accurate Base-Space and Color-Space...
opus4.kobv.de
The majority of next-generation sequencing short-reads can be properly aligned by leading aligners at high speed. However, the alignment quality can still be...
GI JOE STOP MOTION FILM FESTIVAL
www.pondpatrol.com
"Aloha Means Goodbye" - by Carl Piermarini and Jack Celli - USA. "Die Leiden des Action Werthers" - by Bernt Popp - GERMANY. "4:20" - by ...
Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic...
research.rug.nl
... and Breman, {Amy M} and Smith, {Janice L} and Nicholas Katsanis and Bret Bostwick and Bernt Popp and Davis, {Erica E} and Yaping Yang and {Deciphering ...
Improving genetic diagnosis in Mendelian disease with transcriptome...
macarthurlab.org
1 thought on “Improving genetic diagnosis in Mendelian disease with transcriptome sequencing – a walk through”. Bernt Popp says:.
Institute of Human Genetics - Submitter - ClinVar
www.ncbi.nlm.nih.gov
ClinVar archives and aggregates information about relationships among variation and human health.
Is MED13L-related intellectual disability a recognizable syndrome? -...
pure.au.dk
... Denmark., Antje Wiesener, Institute of Human Genetics, University of Erlangen-Nürnberg, Germany., Bernt Popp, Institute of Human Genetics, ...
Is MED13L-related intellectual disability a recognizable syndrome?...
portal.findresearcher.sdu.dk
... Maria Kibæk, Lone Laulund, Niels Illum, Ulrike Dunkhase-Heinl, Antje Wiesener, Bernt Popp, Giuseppe Marangi, Tina Duelund Hjortshøj, Jakob Ek, Ida Vogel, ...
Locus Specific Database list
grenada.lumc.nl
Global Variome shared LOVD https://databases.lovd.nl/shared/genes/GRIN2B, Bernt Popp Institute of Human Genetics, Friedrich-Alexander-Universität ...
NAA10 mutation causing a novel intellectual disability syndrome with...
cyberleninka.org
De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females Bernt Popp, Svein I Støve, ...
Lebensrettender Herzklappen-Ersatz - PDF Kostenfreier Download
docplayer.org
Stock, Hörsaal der Radiologie Zeit: 15:45 Uhr Referent: Bernt Popp, Erlangen 1 Fortbildungspunkt der Bayerischen Landesärztekammer Information: Dr. Jens ...
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