1
0
0
(1 - 15 von 16
)
Hemizygous variants in protein phosphatase 1 regulatory ...Oxford Academic
academic.oup.com
von Z Liu · — Kirsten Cremer ,. Kirsten Cremer. Institute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn. , Bonn. ,. Germany.
Variants in FGF10 cause early onset of severe childhood ...Wiley Online Library
onlinelibrary.wiley.com
von K Schütz · · Zitiert von: 2 — ... Kirsten Cremer MD,. Kirsten Cremer MD. Institute of Human Genetics, School of Medicine & University Hospital Bonn, University of Bonn, Bonn ...
The American Journal of Human Genetics | Vol 97, Issue 3, Pages...
www.sciencedirect.com
De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment. Maja Hempel, Kirsten Cremer, Charlotte W. Ockeloen, Klaske D.
Microdeletions in 9q33.3-q in Molecular Cytogenetics
molecularcytogenetics.biomedcentral.com
von JK Ehret · · Zitiert von: 14 — Julia K. Ehret, Hartmut Engels, Kirsten Cremer, Jessica Becker, Johannes P. Zimmermann, Eva Wohlleber, Elisabeth Mangold, Stefanie Schön, ... › ...
Loss-of-function variants in HIVEP2 are a cause ...Nature Journal
www.nature.com
von S Srivastava · · Zitiert von: 46 — Hartmut Engels, Kirsten Cremer, Martina Kreiß & Alexander M Zink. Institute of Human Genetics, University Hospital Magdeburg, Magdeburg ...
PEDIA: prioritization of exome data by image analysis | Genetics in...
www.nature.com
Department of Human Genetics, University Hospital of Bonn, Bonn, Germany. Kirsten Cremer MD; & Markus Nöthen MD ...
New insights into the clinical and molecular spectrum of the novel...
www.nature.com
— Jessica Becker PhD, Kirsten Cremer MD & Hartmut Engels PhD. Institute of Human Genetics, Universitätsklinikum Hamburg-Eppendorf, Hamburg, ... › articles
Clinical genomics: Institute of Medical and Human GeneticsInstitut für Medizinische Genetik und Humangenetik
genetik.charite.de
... Kirsten Cremer, Magdalena Danyel, Svenja Daschkey, Hilda David Eden, Koenraad Devriendt, Sandra Wilson, Sofia Douzgou, Dejan Đukić, Nadja Ehmke, Christine ...
De Novo Mutations in CHAMP1 Cause Intellectual ...Europe PMC
europepmc.org
von M Hempel · · Zitiert von: 84 — ... Kirsten Cremer. 2Institute of Human Genetics, University of Bonn, Bonn, Germany. Find articles by Kirsten Cremer. Charlotte W. Ockeloen. 3Department of ...
Download Figures (PPT) - Genetics in Medicinegimjournal.org
www.gimjournal.org
... Kirsten Cremer, MD, Robert Day, PhD, Anne-Sophie Denommé-Pichon, MD, Dave A. Dyment, MD, Hartmut Engels, PhD, Rachel Fisher, MS, CGC, Elaine S. Goh, MD ...
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent...
www.infona.pl
Kirsten Cremer. University of Bonn, Institute of Human Genetics, Bonn, Germany. Previous. 1; 2 · 3 · 4 · Next · Terms of service; Accessibility ...
De novo MECP2 duplication in two females with random X-inactivation...
www.bionity.com
De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardation
European Journal of Human Genetics advance online...
PEDIA: prioritization of exome data by image analysis.Europe PMC
europepmc.org
von TC Hsieh · · Zitiert von: 78 — ... Kirsten Cremer. 12Department of Human Genetics, University Hospital of Bonn, Bonn, Germany. Find articles by Kirsten Cremer. Magdalena Danyel. 2Charité ...
HUMAN MOLECULAR GENETICSOxford Academic
academic.oup.com
— ... Kirsten Cremer , Hartmut Engels ,. Sophia O. Peters , Maha S. Zaki , Ruizhi Duan , Changlian Zhu , Yiran Xu , Chao Gao , Tania Sepulveda ...
Unsere Ärztinnen & Ärzte - Institut für Humangenetikhumangenetics-bonn.de
www.humangenetics-bonn.de
— Kirsten Cremer. Fachärztin für Humangenetik – 287 – Dr. med. Tim Bender. Assistenzarzt – 287 – ...
Alle Infos zum Namen "Kirsten Cremer"
sortiert nach Relevanz / Datum