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Phenotype and 244k array-CGH characterization of chromosome 13q...
publichealth.ku.dk
... Gillessen-Kaesbach and Jean-Pierre Fryns and Hanne Rose and Liliana Grozdanova and Ivan Ivanov and Kathelijn Keymolen and Christina Fagerberg and ...
Bücher
DNB, Katalog der Deutschen Nationalbibliothek
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WebPancreas and gallbladder agenesis in a newborn with semilobar holoprosencephaly, a case report / by Robert Hilbrands, Kathelijn Keymolen, Alex Michotte, Miriam Marichal, Filip …
Kathelijn Keymolen | OncoRNALab
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Kathelijn Keymolen Latest Improved Molecular Diagnostics of Idiopathic Short Stature and Allied Disorders: Quantitative Polymerase Chain Reaction-Based Copy Number Profiling ofSHOXand Pseudoautosomal Region 1
Floating harbor syndrome associated with middle ear abnormalities
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Hendrickx , Jan-Jaap, Kathelijn Keymolen, Brigitte Desprechins, Jan Casselman, and Frans Gordts “Floating Harbor Syndrome ...
Dokumente zum Namen
Pregnancy outcome in carriers of Robertsonian translocations
onlinelibrary.wiley.com
9. Sept · Kathelijn Keymolen. ; Department of Gynaecology and Obstetrics, UZ Brussel, Belgium. UZ Brussel, Laarbeeklaan 101, Brussels, Belgium.Search for more papers by this author
Kathelijn KEYMOLEN Reproductive counselling in translocation...
healthcampus.brussels
Kathelijn Keymolen was born in Asse on 10th of November She attended the Koninklijk Atheneum Asse and graduated summa cum laude from Medical School at the VUB in She was trained as a paediatrician in the Sint Pieter and UZ Brussel hospitals in Brussels. During her training in paediatrics, she spent one year in the Centre
Kathelijn Keymolen - Academia.edu
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Wissenschaftliche Veröffentlichungen
Journal of the Neurological Sciences | Vol 308, Issues 1–2, Pages...
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... electromyography findings on room temperature. Pages Véronique Bissay, Kathelijn Keymolen, Willy Lissens, Eric Schmedding, Jacques De Keyser.
Late onset painful cold-aggravated myotonia: Three families with...
www.sciencedirect.com
... Brussel, Vrije Universiteit Brussel (VUB), Laarbeeklaan 101, B1090 Brussels, Belgium. Tel.: + ; fax: + email. ,. Kathelijn Keymolen.
Veröffentlichungen allgemein
Early onset Huntington disease: a neuronal degeneration syndrome |...
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Kathelijn Keymolen Æ Willy Lissens Æ Daniele Hasaerts. Sara Debulpaep Æ Brigitte Desprechins Æ Inge Liebaers. Linda De Meirleir.
Artikel & Meinungen
A prospective study of the clinical utility of prenatal chromosomal...
www.nature.com
Original Research Article
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Kathelijn Keymolen — Vrije Universiteit Brussel
researchportal.vub.be
Fingerprint. Dive into the research topics where Kathelijn Keymolen is active. These topic labels come from the works of this person. Together they form a unique fingerprint. 1 Similar Profiles. Mutation Medicine & Life Sciences. 100%. Genetic Testing Medicine & Life Sciences. 60%.
Kathelijn Keymolen's research works | University Hospital...
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Kathelijn Keymolen's 58 research works with 1,770 citations and 9,753 reads, including: Searching for a sense of closure: parental experiences of recontacting after a terminated pregnancy for ...
dr. Kathelijn Keymolen - Centrum voor Zeldzame Ziekten - UZ...
www.uzbrussel.be
Dr. Kathelijn Keymolen is afgestudeerd als pediater aan de Vrije Universiteit Brussel en is sinds erkend als klinisch geneticus. Ze werkt sinds in het Centrum medische genetica en behaalde een doctoraat met betrekking tot de reproductieve counseling van dragers van structurele chromosomale afwijkingen. Terug.
dr. Kathelijn Keymolen - Genetics - UZ Brussel
www.uzbrussel.be
About Dr. Kathelijn Keymolen. Dr. Kathelijn Keymolen graduated as a paediatrician at the Free University of Brussels and since has been qualified as a clinical geneticist. Since she has been working in the Centre for Medical Genetics and obtained a doctorate relating to the reproductive counselling of carriers of structural ...
dr. Kathelijn Keymolen - von Hippel-Lindau Expert Center (VHL
www.uzbrussel.be
dr. Kathelijn Keymolen - von Hippel-Lindau Expert Center (VHL) - UZ Brussel dr. Kathelijn Keymolen Genetica Care provider under the health care... Navigation
Génétique clinique
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WebNuméro d'entreprise: Comité directeur. Présidente : Kathelijn KEYMOLEN Vice-président : Damien LEDERER Secrétaire : Bruce POPPE
Researcher: Kathelijn Keymolen in Publications - Dimensions
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Re-imagining discovery and access to research: grants, datasets, publications, citations, clinical trials, patents and policy documents in one place.
Kathelijn Keymolen – Research output — Vrije...
researchportal.vub.be
Expanding the clinical spectrum of biallelic ZNF335 variants · Stouffs, K., Stergachis, A. B., Vanderhasselt, T., Dica, A., Janssens, S., Vandervore, L., Gheldof, A., ...
(PDF) Post-zygotic origin of isochromosome 12p | Kathelijn Keymolen -...
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Post-zygotic origin of isochromosome 12p
CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased...
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Lise Barbé, Stella Lanni, Arturo López-Castel, Silvie Franck, Claudia Spits, Kathelijn Keymolen, Sara Seneca, Stephanie Tomé, Ioana Miron, ...
June 20, Issue of JAMA Dermatology | JAMA Network
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Read the June 20, issue. Volume 147, Number 6
Minerva Pediatrica June;70(3) - Minerva Medica - Riviste
www.minervamedica.it
Melissa SYS *, Ann van den BOGAERT, Bram ROOSENS, Annik LAMPO, Anna JANSEN, Sara WOUTERS, Kathelijn KEYMOLEN. Abstract PDF. ORIGINAL ...
Post-zygotic origin of isochromosome 12p. — NextBio article
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Thomy J L de Ravel, Kathelijn Keymolen, Elvire van Assche, Ingrid Wittevronghel, Philippe Moerman, Ivo Salden, Gert Matthijs, Jean-Pierre Fryns, Joris R ...
(PDF) Two different infantile phenotypes of Rett syndromes |...
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Two different infantile phenotypes of Rett syndromes
Polyneuropathy in a young Belgian patient: A novel heterozygous...
ng.neurology.org
Jeroen de Filette,; Danielle Hasaerts, MD,; Sara Seneca, PhD,; Alexander Gheldof, PhD,; Katrien Stouffs, PhD,; Kathelijn Keymolen, MD and ...
Post-zygotic origin of isochromosome 12p | Read by QxMD
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Thomy J L de Ravel, Kathelijn Keymolen, Elvire van Assche, Ingrid Wittevronghel , Philippe Moerman, Ivo Salden, Gert Matthijs, Jean-Pierre Fryns, Joris R ...
SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap...
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Véronique Bissay, Sophie C H Van Malderen, Kathelijn Keymolen, Willy Lissens, Uschi Peeters, Dorien Daneels, Anna C Jansen, Gudrun Pappaert, Pedro ...
Mito DB
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... Valerie Cormier-Daire, Barbara Crandall, Katariina Hannula-Jouppi, Raoul Hennekam, Denise Herzog, Kathelijn Keymolen, Marita Lipsanen-Nyman, Peter ...
Phenotype and 244k array-CGH characterization of chromosome 13q...
di.ku.dk
... Hanne Rose ; Liliana Grozdanova ; Ivan Ivanov ; Kathelijn Keymolen ; Christina Fagerberg ; Lisbeth Tranebjaerg ; Flemming Skovby ; Margarita Stefanova.
(PDF) The mutation spectrum in RECQL4 diseases | Abdelmadjid...
www.academia.edu
The mutation spectrum in RECQL4 diseases
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