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A familial disorder of altered DNA-methylation | Journal of Medical...
jmg.bmj.com
Almuth Caliebe Institute of Human Genetics, University Hospital Schleswig-Holstein Campus Kiel/Christian-Albrechts University Kiel, Kiel, ...
A familial disorder of altered DNA-methylation - JMG Contact blog
blogs.bmj.com
... disorder of genomic imprinting. (By Dr. med. Almuth Caliebe, http://jmg.bmj.com/content/early jmedgenet ) ...
Firmen-Mitarbeiter
Preisträger | GfH - Deutsche Gesellschaft für Humangenetik e.V.
gfhev.de
Preisträger GfH-Vortragspreis Almuth Caliebe für die Mitautoren Frohnauer J, Gesk S, Siebert R, Pankau ...
Bücher
STXBP1 encephalopathy : a neurodevelopmental disorder including...
biblio.ugent.be
... Willemsen, Patrizia Accorsi, Marco Angriman, Hartmut Baier, Ira Benkel- Herrenbrueck, Valérie Benoit, Mauro Budetta, Almuth Caliebe, et al.
Almuth Caliebe | XanEdu Customization Platform
www.academicpub.com
Author: Almuth Caliebe. Results. Dyschromatosis ptychotropica: an unusual pigmentary disorder in a boy with epileptic encephalopathy and progressive atrophy ...
Nachweis des CD30-Membranantigens und der kreuzreagierenden...
books.google.de
Almuth Caliebe pages. 0 Reviewshttp://books.google.com/books/about/Nachweis_des_CD30_Membranantigens_und_de.html?id=s_yEYgEACAAJ ...
Dokumente zum Namen
EBSCOhost | | A familial disorder of altered DNA-methylation.
web.b.ebscohost.com
Almuth Caliebe,1 Julia Richter,1 Ole Ammerpohl,1 Deniz Kanber,2 Jasmin Beygo,2. Susanne Bens,1 Andrea Haake,1 Eva Jüttner,3 Bernhard ...
Störungen der Geschlechts entwicklung - Netzwerk DSD
www.netzwerk-dsd.uk-sh.de
Dr. Almuth Caliebe Oberärztin des Instituts für Humangenetik Sprechstunden Ellen Kröger Klinik für Allgemeine Pädiatrie
Exome sequencing unravels unexpected differential diagnoses in...
www.deepdyve.com
Koray Boduroglu · Diana Braunholz · Almuth Caliebe · Krystyna H. Chrzanowska · Johanna Christina Czeschik ·. Sabine Endele · Elisabeth ...
DeepDyve - Unlimited Access to Peer-Reviewed Journals
www.deepdyve.com
DeepDyve is the largest online rental service for scholarly research with thousands of academic publications available at your fingertips.
Wissenschaftliche Veröffentlichungen
Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of...
www.sciencedirect.com
School, and Harvard Stem Cell Institute, Boston, MA , USA. ,. Almuth Caliebe. x.
Partial Hydatidiform Mole With Extensive Angiomatoid Vessel Confi...:...
www.ingentaconnect.com
Vessel Configuration in a First Trimester Miscarriage. Henning Feist, M.D., Almuth Caliebe, M.D., Jennifer Oates, M.D.,. Nanette Sarioglu, M.D., and Kais Hussein ...
Conflicting results of prenatal FISH with different probes for Down's...
molecularcytogenetics.biomedcentral.com
... Stefan Gesk, Inga Nagel, Andrea Haake, Susanne Bens, Simone Heidemann, Monika Kautza, Christian Timke, Reiner Siebert and Almuth Caliebe.
Klinik für Dermatologie | Kiel
www.dermatology.uni-kiel.de
PD Dr. Almuth Caliebe, ; Labor (mit Ringversuchszertifikat) Prof. Dr. Ralf Junker, ; Selbsthilfevereinigungen
Veröffentlichungen allgemein
A comprehensive molecular study on Coffin-Siris and...
core.ac.uk
... Beate Albrecht, Koray Boduroglu, Almuth Caliebe, Krystyna Chrzanowska, Ozgur Cogulu, Francesca Cristofoli, Johanna ... Publisher: Oxford University Press.
Cleidocranial dysplasia with decreased bone density and biochemical...
link.springer.com
(A1); Judit Kárteszi (A1); János Weisenbach (A2); Almuth Caliebe (A3); Stefan Mundlos (A4); Károly Méhes (A1). Author Affiliations. A1. Department of Medical ...
Almuth Caliebe - Wikidata
www.wikidata.org
Almuth Caliebe (Q ). From Wikidata. Jump to navigation Jump to search . No description defined. edit. Language, Label, Description, Also known as ...
Artikel & Meinungen
Listenansicht
www.kieler-aerzteverein.de
Kieler Ärzteverein e.V. - Informationen, Veranstaltungen und mehr. Von Ärzten für Ärzte. Besuchen Sie uns auf www.kieler-aerzteverein.de!
Mutations in STX1B, encoding a presynaptic protein, cause...
www.nature.com
Holger Lerche, Camila Esguerra and colleagues report the identification of inactivating mutations in STX1B in individuals with various seizure-related...
Sonstiges
Dr.med. Almuth Caliebe in Kiel FA für Humangenetik - ärzte.de |...
www.aerzte.de
➤ Dr.med. Almuth Caliebe in Kiel FA für Humangenetik ➤ Bewertungen, Leistungen, Telefonnummern, Öffnungszeiten, Online Wunsch-Termin ➤ Jetzt klicken!
LIVIVO - Search results - AU="Caliebe, Almuth"
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LIVIVO - The Search portal for Life Sciences
AKT3 - Labome.Org
www.labome.org
Almuth Caliebe Studies, School of Medicine, University of Manchester, G 38, Stopford Building, Oxford Road, M13 9PT, Manchester, UK
Aviso
dre.tretas.org
º 9 00, Oxford University Press; ... Haake, Susanne Bens, Simone Heidemann, Monika Kautza, Christian Timke, Reiner Siebert, Almuth Caliebe.
Nöldeke.de
www.nöldeke.de
Am Freitag, um 15 Uhr s. t. hält Dr. med. Almuth Caliebe ihre Antrittsvorlesung zu dem Thema "Der Apfel fällt nicht weit vom Stamm" ...
Array based DNA methylation profiling in male infertility reveals...
www.fertstertdialog.com
Array-based DNA-methylation profiling identifies 471 CpGs as markers for idiopathic infertility in peripheral blood and suggests allele-specific DNA...
Catel Manzke Syndrome - NORD (National Organization for Rare...
rarediseases.org
Catel Manzke Syndrome. NORD gratefully acknowledges Almuth Caliebe, MD, Institute of Human Genetics, University Hospital Schleswig-Holstein, Campus ...
Prof.Dr.med. Reiner Siebert in Kiel FA für Humangenetik -...
www.aerzte.de
➤ Prof.Dr.med. Reiner Siebert in Kiel FA für Humangenetik ➤ Bewertungen, Leistungen, Telefonnummern, Öffnungszeiten, Online Wunsch-Termin ➤ Jetzt klicken!
DNA-Methylation Profiling of Fetal Tissues Reveals Marked Epigenetic...
journals.plos.org
Almuth Caliebe, ... Bens S, Kolarova J, Schneppenheim S, Caliebe A, Heidemann S, et al. (2012) Oxford University Press New York p.
A familial disorder of altered DNA-methylation | Read by QxMD
read.qxmd.com
Almuth Caliebe, Julia Richter, Ole Ammerpohl, Deniz Kanber, Jasmin Beygo, Susanne Bens, Andrea Haake, Eva Jüttner, Bernhard Korn, Deborah J G Mackay, ...
Deep Bisulfite Sequencing of Aberrantly Methylated Loci in a Patient...
figshare.com
Deep Bisulfite Sequencing of Aberrantly Methylated Loci in a Patient with Multiple Methylation Defects
Haploinsufficiency of a Spliceosomal GTPase Encoded by EFTUD2 Causes...
cyberleninka.org
... Baujat,6 Denise Horn,7 Usha Kini,8 Almuth Caliebe,9 Yasemin Alanay,10, Oxford Radcliffe Hospitals National Health Service Trust, Oxford OX3 7LJ, UK; ...
Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of...
www.infona.pl
Almuth Caliebe. Institute of Human Genetics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, ...
Dyschromatosis ptychotropica: an unusual pigmentary disorder in a boy...
www.infona.pl
Ingo Helbig, Regina Fölster-Holst, Jochen Brasch, Ingrid Hausser, Andreas van Baalen, Hiltrud Muhle, Karsten Alfke, Almuth Caliebe, … [ more ].
Gesa Schwanitz| International Journal of Molecular Genetics and Gene...
www.sciforschenonline.org
Dr. Gesa Schwanitz was born at Müncheberg, Germany in She completed her Diploma in h. c. Semmelweis University Budapest, Hungary.
Mutations in STX1B, encoding a presynaptic protein, cause...
www.bionity.com
Rüschendorf, Almuth Caliebe, Inga Nagel, Bernard Kohl, Angela ...
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