Interests
Telomere shortening protects against cancer - ScienceDaily
www.sciencedaily.com
Dec 1, — Isabelle Schmutz, Arjen R Mensenkamp, Kaori K Takai, Maaike Haadsma, Liesbeth Spruijt, Richarda M de Voer, Seunga Sara Choo, ... › releases ›
Scholten Awater Zevenheuvelenloop | Uitslag Liesbeth Spruijt
evenementen.uitslagen.nl
Naam, Liesbeth Spruijt. Woonplaats / vereniging, Nijmegen. Afstand, Zevenheuvelennacht - 7 km. Categorie, V45. Totaal plaats, Categorie plaats, Snelheid, km/uur. Nettotijd, 43:50. Bruto tijd, 56:
C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome |...
jmg.bmj.com
Liesbeth Spruijt,. 1. Elisabeth A M Cornelissen,. 4. Janneke H M Schuurs-Hoeijmakers,1,2,3 Nicole de Leeuw,1,2,3 Valérie Cormier-Daire,5.
Business Profiles
Liesbeth Spruijt Radboud University Medical Centre ...
www.researchgate.net
› profile › Liesbeth-Spruijt
Education
Liesbeth SPRUIJT - Copains d'avant
copainsdavant.linternaute.com
Liesbeth SPRUIJT est sur Copains d'avant. Pour la contacter, connectez-vous ou inscrivez-vous gratuitement.
Books & Literature
Pathogenetics of alveolar capillary dysplasia with ...
biblio.ugent.be
by P Szafranski · · Cited by 67 — ... Eileen Mckay, Nicole de Leeuw, Ilse Feenstra, Liesbeth Spruijt, Frances Elmslie, Timothy Thiruchelvam, Carlos A Bacino, Claire Langston, ... › publication
Hereditary Tumors: From Genes to Clinical Consequences
books.google.com
Liesbeth Spruijt and Nicoline Hoogerbrugge Summary A hereditary predisposition to renal cell cancer (RCC) is suspected when a patient with RCC has a ...
The Three Pillars of Evolution Demolished: Why Darwin Was Wrong
books.google.com
Zeegers, Maurice P.A., Frans van Poppel, Robert Vlietinck, Liesbeth Spruijt, and Harry Ostrer Founder mutations among the Dutch.
Cengage Advantage Books: Culture Counts: A Concise ...
books.google.de
Zeegers, Maurice, Frans van Poppel, Robert Vlietinck, Liesbeth Spruijt, and Harry Ostrer “Founder Mutations among the Dutch.” European Journal of ...
Related Documents
ARTICLE - CiteSeerX
citeseerx.ist.psu.edu
by AJH Genet · · Cited by 370 — Gavin Hudson, Valerio Carelli, Liesbeth Spruijt, Mike Gerards, Catherine Mowbray,. Alessandro Achilli, Angela Pyle, Joanna Elson, Neil Howell, ... › viewdoc › download
C14ORF179 encoding IFT43 is mutated in ProQuest
search.proquest.com
by HH Arts · · Cited by 146 — Liesbeth Spruijt,. 1. Elisabeth A M Cornelissen,. 4. Janneke H M Schuurs-Hoeijmakers,1,2,3 Nicole de Leeuw,1,2,3 Valérie Cormier-Daire,5. Han G Brunner,. by RDA Weren · · Cited by 33 — Liesbeth Spruijt,1 Jan Lubinski,3 Anna Jakubowska,3 Urszula teodorczyk,3. Cora M Aalfs,4 Liselotte p van hest,5 Carla oliveira,6,7,8 eveline J Kamping,1. › openview › 1.pdf
Highly Variable Phenotype of LZTR1 Schwannomatosis ...
meeting.peripheralnerve.org
Back to Annual Meeting Program. Highly Variable Phenotype of LZTR1 Schwannomatosis Includes Neurofibromas Justus L Groen, MD PhD1; Liesbeth Spruijt, ... › abstracts
Medline ® Abstracts for References of 'Lynch syndrome ...
www.uptodate.com
... Arjen R. Mensenkamp, and Liesbeth Spruijt, Radboud University Medical Center, Nijmegen; Fred H. Menko, Vrije Universiteit, University Medical Center; ... › contents › abstract
Scientific Publications
Neurofibromas in LZTR1 schwannomatosis - PubMed
pubmed.ncbi.nlm.nih.gov
Feb 17, — Justus L Groen , Setareh Moghadasi , Liesbeth Spruijt , Esther Korpershoek , Yvette van Ierland , J Tom van Wezel , Sjoerd van Duinen ... by SW Ten Broeke · · Cited by 4 — ... J W Olderode-Berends , Jenny von Salomé , Hans K Schackert , Liesbeth Spruijt , Verena Steinke-Lange , Anja Wagner , Carli M J Tops , Maartje Nielsen ... › ...
DNA-testing for BRCA1/2 prior to genetic counselling in ...
bmcwomenshealth.biomedcentral.com
by AS Sie · · Cited by 11 — Liesbeth Spruijt,; Wendy AG van Zelst-Stams,; Arjen R Mensenkamp,; Marjolijn J Ligtenberg,; Han G Brunner ... › articles
Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner...
www.ncbi.nlm.nih.gov
Christian Gilissen, 1, 3 Heleen H. Arts, 1, 3 Alexander Hoischen, 1, 3 Liesbeth Spruijt, 1 Dorus A. Mans, 1 Peer Arts, 1 Bart van Lier, 1 Marloes Steehouwer, 1 Jeroen ...
Pancreatic cancer-associated gene polymorphisms in a nation-wide...
bmcresnotes.biomedcentral.com
Thomas P PotjerEmail author,; Nienke van der Stoep,; Jeanine J Houwing-Duistermaat,; Ingrid C A W Konings,; Cora M Aalfs,; Peter C van den Akker,; Margreet G Ausems,; Charlotte J Dommering,; Lizet E van der Kolk,; Merel C Maiburg,; Liesbeth Spruijt,; Anja Wagner,; Hans F A Vasen and; Frederik J Hes. BMC Research ...
Publications
Report Identification of an X-Chromosomal Locus and CORE
core.ac.uk
by G Hudson · · Cited by 194 — Rita Horvath,7 Veronika Karcagi,8 Liesbeth Spruijt,9 I. F. M. de Coo,9,10. Hubert J. M. Smeets,9 and Patrick F. Chinnery1,3. › download › pdf
SNP association study in PMS2-associated Lynch syndrome
link.springer.com
by SW ten Broeke · · Cited by 6 — Arjen R. Mensenkamp & Liesbeth Spruijt. Department of Clinical Genetics, Academic Medical Centre, Amsterdam, The Netherlands. › article
Clinical Expression of Leber Hereditary Optic Neuropathy Is Affected...
core.ac.uk
By Gavin Hudson, Valerio Carelli, Liesbeth Spruijt, Mike Gerards, Catherine Mowbray, Alessandro Achilli, Angela Pyle, Joanna Elson, Neil Howell, Chiara ...
Video & Audio
YouTube
www.youtube.com
Auf YouTube findest du großartige Videos und erstklassige Musik. Außerdem kannst du eigene Inhalte hochladen und mit Freunden oder mit der ganzen Welt teilen.
Reports & Statements
CORRIGENDa aND ERRaTa - Nature
www.nature.com
Nils Rahner, MD, PhD, Bert J. W. Redeker, PhD, M.J.W. Olderode-Berends, MD, PhD, Liesbeth Spruijt, MD, PhD, Yvonne J. Vos, PhD,. Anja Wagner, MD, PhD, ... › articles › gim
Miscellaneous
Liesbeth Spruijt | LinkedIn
www.linkedin.com
View Liesbeth Spruijt's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Liesbeth Spruijt discover ...
C 14 ORF 179 encoding IFT 43 is mutated in Sensenbrenner ...
www.academia.edu
... Dorus Mans, Sylvia van Beersum, Machteld Oud, Emine Bolat, Liesbeth Spruijt, Elisabeth Cornelissen, Janneke Schuurs-Hoeijmakers, Nicole de Leeuw, et al. › C_14_ORF_179_encoding...
Ciliopathies with skeletal anomalies and renal insufficiency ...
read.qxmd.com
Heleen H Arts, Ernie M H F Bongers, Dorus A Mans, Sylvia E C van Beersum, Machteld M Oud, Emine Bolat, Liesbeth Spruijt, Elisabeth A M Cornelissen, ... › read › ciliopathies-with-skeleta...
Clinical Phenotype of 5 Females With a CDKL5 Mutation
journals.sagepub.com
by XL Stalpers · · Cited by 23 — Xenia L. Stalpers, MD, MSc1, Liesbeth Spruijt, MD, PhD2,. Helger G. Yntema, PhD2, and Aad Verrips, MD, PhD1. Abstract. Mutations in the X-linked cyclin ... › doi › pdf
Clinical expression of leber hereditary optic neuropathy is ...
moh-it.pure.elsevier.com
by G Hudson · · Cited by 370 — Gavin Hudson, Valerio Carelli, Liesbeth Spruijt, Mike Gerards, Catherine Mowbray, Alessandro Achilli, Angela Pyle, Joanna Elson, Neil Howell, ... › publications › clinical...
DNA-testing for BRCA1/2 prior to genetic counselling in ...
cyberleninka.org
Similar topics of scientific paper in Clinical medicine , author of scholarly article — Aisha S Sie, Liesbeth Spruijt, Wendy AG van Zelst-Stams, Arjen R ... › article
Germline Mutations in the Spindle Assembly Checkpoint ...
www.gastrojournal.org
by RM de Voer · · Cited by 105 — MAAYKE ARIAANS,1 LIESBETH SPRUIJT,1 TON VAN ESSEN,5 GUNNAR HOUGE,6 HANS K. SCHACKERT,7 JIAN Q. SHENG,3. HANKA VENSELAAR,8 CONNY M. A. VAN RAVENSWAAIJ–ARTS, › article › pdf
Identification of Novel Candidate Genes for Early Figshare
figshare.com
Feb 22, — ... Arjen R. Mensenkamp, Christian Gilissen, Wendy A. van Zelst-Stams, Liesbeth Spruijt, C. Marleen Kets, Junxiao Zhang, Hanka Venselaar, ... › articles › dataset › Identification_...
Identification of Novel Candidate Genes for Early-Onset ...
journals.plos.org
Feb 22, — Liesbeth Spruijt,. Affiliation Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands. › article › comments › journal....
Influence of Mutation Type on Clinical Expression of Leber ...
www.ajo.com
by L Spruijt · · Cited by 133 — Inquiries to Liesbeth Spruijt, MD, Maastricht University, Department of Clinical Genetics/Genetics and Cell Biology, Universiteitssingel 50,. › article › pdf
Molecular Background of Colorectal Tumors From Patients ...
researchportal.vub.be
by SW Ten Broeke · · Cited by 29 — ... Maran J W Olderode-Berends, Dina Ruano, Liesbeth Spruijt, Manon Suerink, Carli M Tops, Ronald van Eijk, Hans Morreau, Tom van Wezel, Maartje Nielsen. › publications › molecular...
Sequence analysis of the mitochondrial genomes from Dutch ...
research-repository.uwa.edu.au
Neil Howell, Roelof Jan Oostra, Piet A. Bolhuis, Liesbeth Spruijt, Lorne A. Clarke, David A. Mackey, Gwen Preston, Corinna Herrnstadt. › fingerprints
TINF2 is a haploinsufficient tumor suppressor that limits eLife
elifesciences.org
by I Schmutz · · Cited by 8 — Liesbeth Spruijt. Department of Human Genetics, Radboud University Medical Center, Nijmegen, Netherlands ... › articles
The apparent genetic anticipation in PMS2-associated Lynch ...
vbn.aau.dk
by SW Ten Broeke · · Cited by 4 — ... Pål Møller, Theo A M van Os, Marta Pineda, Nils Rahner, Maran J W Olderode-Berends, Jenny von Salomé, Hans K Schackert, Liesbeth Spruijt Show 4 more › publications › the-apparent-genetic...
The effect of genotypes and parent of origin on cancer risk and ...
www.gimjournal.org
... MD, PhD, Bert J. W. Redeker, PhD, M.J.W. Olderode-Berends, MD, PhD, Liesbeth Spruijt, MD, PhD, Yvonne J. Vos, PhD, Anja Wagner, MD, PhD, Hans Morreau, ... › article › fulltext
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