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heiBIB: Fischer, ChristineHeidelberg University
katalog.ub.uni-heidelberg.de
... Roland Schmid, Hana Algül, Philipp J. Jost, Juliane Ramser, Christine Fischer, Anne S. Quante, Maximilian Reichert, and Michael Quante, March 25, › profil
The Human Genome Project: Hearing Before the Subcommittee on ...books.google.com › books
books.google.de
... Bethesda , MD , USA Dr. Juliane Ramser , Max - Planck - Institut fur Moleculare Genetik , Berlin , Germany Dr. Bruce Roe , University of Oklahoma ...
unique exonic splice enhancer mutation in a family with X ...Oxford University Press
academic.oup.com
von J Ramser · · Zitiert von: 216 — A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor. Juliane Ramser,. › hmg
BRIP1 loss-of-function mutations confer high risk for familial...
breast-cancer-research.biomedcentral.com
· Juliane Ramser, Eva Groß & Alfons Meindl. Department of Human Genetics, University Würzburg, Biozentrum, Würzburg, Germany.
An ENIGMA resource to support clinical variant classification – ...The University of Western Australia
research-repository.uwa.edu.au
... Nicola K. Poplawski, Berardino Porfirio, Anne S. Quante, Juliane Ramser, Rui M. Reis, Françoise Revillion, Kerstin Rhiem, Barbara Riboli, Julia Ritter, ... › ...
Association of genomic domains in BRCA1 and BRCA2 with prostate...
pure.au.dk
... Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy. ,; Juliane Ramser, Department of Gynaecology and Obstetrics, Technical University Munich.
A physical map of the human genome — Keio University
keio.pure.elsevier.com
... Jun Kudoh ; Shinsei Minoshima ; Juliane Ramser ; Peter Seranski ; Celine Hoff ; Annemarie Poustka ; Richard Reinhardt ; Hans Lehrach.
Chromosome specific 4q matrix-CGH chip to refine the ...AACR Journals
aacrjournals.org
von CM Simbulan-Rosenthal · — Juliane Ramser;. Juliane Ramser. Department of Gynecol. & Obstetrics University Hosp. Schleswig Holstein Campus Kiel, Kiel, Germany, ... › article
Hailey-Hailey disease is caused by mutations in ATP2C1 ...University of Southampton
eprints.soton.ac.uk
von R Sudbrack · · Zitiert von: 385 — Contributors · Ralf Sudbrack · Joanna Brown · Carol Dobson-Stone · Simon Carter · Juliane Ramser · Jacqueline White · Eugene Healy · Manuel Dissanayake. › ...
Initial sequencing and analysis of the human genome – FingerprintThe University of Manchester
research.manchester.ac.uk
... Michael J. Proctor, Bruce A. Roe, Feng Chen, Huaqin Pan, Juliane Ramser, Hans Lehrach, Richard Reinhardt, W. Richard McCombie, Melissa De La Bastide, ... › ...
Rare Missense and Synonymous Variants in UBE1 Are Associated with...
www.infona.pl
Strony Opis fizyczny. Twórcy. autor. Juliane Ramser. Department of Obstetrics and Gynecology, Technical University Munich, Munich, Germany.
The DNA sequence of the human X chromosomeThe University of Edinburgh
www.research.ed.ac.uk
... Stephen Searle, Juliane Ramser, Adam Whittaker, Rebecca Deadman, Nigel P Carter, Sarah E Hunt, Rui Chen, Andrew Cree, Preethi Gunaratne, Paul Havlak, ... › fi...
The reduced expression of the HADH2 protein causes X- ...Monash University
research.monash.edu
von C Lenski · · Zitiert von: 65 — ... Daniela Loessner, Ronald J.A. Wanders, Birgitta Winnepenninckx, Heide Hellebrand, Stefanie Engert, Charles E. Schwartz, Alfons Meindl, Juliane Ramser. › the-...
NCALD as a potential predictive biomarker for the efficacy ...Future Medicine
www.futuremedicine.com
— ... Sabine Grill; &; Juliane Ramser. Sarah M Konrad. Department of Gynecology & Obstetrics, University Hospital rechts der Isar, ... › ...
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