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Heritage
Christian MICHOLT : Family tree by Erik LAMOTE (eriklamote)
gw.geneanet.org
(Chris MICHOLT). Parents. Stefaan Alfons Maria Micholt ; Irena GARMYN. Spouses, children and grandchildren. Married to Martine Biervliet (Parents : ... › eriklamote
Books & Literature
Oculocutaneous albinism type IV: A boy of Moroccan descent ...
onlinelibrary.wiley.com
by T Konno · · Cited by 13 — Martine Biervliet,. Martine Biervliet. Department of Medical Genetics, University and University Hospital of Antwerp, Antwerp, Belgium. by W Wuyts · · Cited by 65 — Wim Wuyts,1,2* Martine Biervliet,2 Edwin Reyniers,2 Maria Rosaria D'Apice,3 Giuseppe Novelli,3 and Katrien Storm2. 1Department of Medical Genetics, ... › doi › abs › ajmg.a › doi › pdf › ajmg.a
Genetic defects in TAPT1 disrupt ciliogenesis and cause a complex ...
biblio.ugent.be
Symoens, Sofie, Aileen M Barnes, Charlotte Gistelinck, Fransiska Malfait, Brecht Guillemyn, Wouter Steyaert, Delfien Syx, Sanne D'hondt, Martine Biervliet, ... by S Symoens · — ... Wouter Steyaert, Eef Parthoens, Martine Biervliet, Gabriele Gillessen-Kaesbach, Julie De Backer, Andy Willaert, Hans Peter Bächinger, ... › publication
Isabelle Pirson - Typeset.io
typeset.io
457 results — Anne Genin, Julie Désir 1, Nelle Lambert 1, Martine Biervliet +9 more•Institutions (2). 12 Sep Human Molecular Genetics. › authors
Defects in TAPT1, involved in axial skeletal patterning, cause a...
biblio.ugent.be
UGent) , Eef Parthoens (UGent) , Martine Biervliet, et al.
Related Documents
Brugada-syndroom - UZ Brussel
www.uzbrussel.be
Dr. Maryse Bonduelle, klinisch geneticus l Dr. Martine Biervliet. LABO CENTRUM MEDISCHE GENETICA l Dr. Sonia van Dooren, labo-coördinator en lab supervisor. › documents › Brugada+...
Erratum to “High incidence of the CFTR mutations A ...
repository.uantwerpen.be
by K Storm · · Cited by 9 — Martine Biervliet a. , Lutgardis Van Schil c. ,. Kristine Desager b. , Markus M. Nöthen a,1 a Department of Medical Genetics, University and ... › docman › irua
Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a ...
europepmc.org
by S Symoens · · Cited by 33 — ... M. Barnes,2,8 Charlotte Gistelinck,1,8 Fransiska Malfait,1 Brecht Guillemyn,1 Wouter Steyaert,1 Delfien Syx,1 Sanne D'hondt,1Martine Biervliet,3 Julie ... › pmc › bin › mmc3
Involvement of PLEKHM1 in osteoclastic vesicular transport ...
www.jci.org
the confocal imaging, Martine Biervliet for taking blood samples, and Kevin Mackenzie, John Greenhorn, Adam Taylor, and Denise. › view › version › pdf › render
Scientific Publications
Genetic Defects in TAPT1 Disrupt Ciliogenesis and PubMed
pubmed.ncbi.nlm.nih.gov
by S Symoens · · Cited by 33 — ... Sanne D'hondt , Martine Biervliet , Julie De Backer , Eckhard P Witten , Sergey Leikin , Elena Makareeva , Gabriele Gillessen-Kaesbach ... › ...
High incidence of the CFTR mutations A → G and L927P in...
www.sciencedirect.com
Katrien Storm, Els Moens, Lieve Vits, Haike De Vlieger, Gino Delaere, Maria D'Hollander, Wim Wuyts, Martine Biervliet, Lutgardis Van Schil, Kristine Desager, Markus M. Nöthen. Erratum to “High incidence of the CFTR mutations A → G and L927P in Belgian cystic fibrosis patients, and identification ...
Publications
N1303K and IVS8-5T, clinical presentation ResearchGate
www.researchgate.net
Martine Biervliet · Martine Biervliet. This person is not on ResearchGate, or hasn't claimed this research yet. Show all 5 authorsHide. › publication
Kinetochore KMN network gene CASC5 mutated in primary microcephaly
core.ac.uk
By Anne Genin, Julie Desir, Nelle Lambert, Martine Biervliet, Nathalie Van Der Aa, Geneviève PIERQUIN, Audrey Killian, Mario Tosi, Montse Urbina, Anne Lefort ...
Kinetochore KMN network gene CASC5 mutated in primary microcephaly
m.wikidata.org
scientific article
Reports & Statements
New ZMPSTE24 (FACE1) mutations in patients Nature
www.nature.com
by CL Navarro · · Cited by 51 — Martine Biervliet. Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands. › ... › articles
Miscellaneous
Genetic Defects in TAPT1 Disrupt Ciliogenesis SlidePlayer
slideplayer.com
Sofie Symoens, Aileen M. Barnes, Charlotte Gistelinck, Fransiska Malfait, Brecht Guillemyn, Wouter Steyaert, Delfien Syx, Sanne D'hondt, Martine Biervliet, ... › slide
MARTINE BIERVLIET, N\A: contacten, telefoonnummer, adres, werk ...
ydo.be
› public › martine-bier...
Dr Martine Biervliet General Practitioner | doctoranytime
www.doctoranytime.be
› ... › Martine Biervliet
Biervliet, Martine: biblioteca eletrónica gratuita Z-Library
pt.booksc.me
Wim Wuyts, Martine Biervliet, Edwin Reyniers, Maria Rosaria D'Apice, Giuseppe Novelli, Katrien Storm. Diário: American Journal of Medical Genetics Part A. › ...
A patient with Baller-Gerold syndrome and midline NK/T ...
read.qxmd.com
H Annika Siitonen, Jenni Sotkasiira, Martine Biervliet, Abdelmadjid Benmansour, Yline Capri, Valerie Cormier-Daire, Barbara Crandall, ... › read › a-patient-with-baller-ge...
Administratieve aspecten - PDF Gratis download - DocPlayer.nl
docplayer.nl
Dr. Em. Inge Liebaers Dr. Marjan De Rademaeker Dr. Kathelijn Keymolen Dr. Martine Biervliet Dr. Kim Van Berkel Dr. Ellen Denayer Coördinatie PGD-kliniek ... › Ad...
Channelpedia - EPFL
channelpedia.epfl.ch
... Lieve Vits, Haike De Vlieger, Gino Delaere, Maria D'Hollander, Wim Wuyts, Martine Biervliet, Lutgardis Van Schil, Kristine Desager, Markus M Nöthen. › pubmeds
CoOccurrence - Aspm - Homo sapiens - BioKB
biokb.lcsb.uni.lu
... Authors: Anne Genin Julie Desir Nelle Lambert Martine Biervliet Nathalie Van Der Aa Genevieve Pierquin Audrey Killian Mario Tosi Montse Urbina Anne ... › ENSRNOP
Het Brugada syndroom - Centrum voor Medische Genetica
studylibnl.com
Dr. Maryse Bonduelle, klinisch geneticus Dr. Martine Biervliet, klinisch geneticus LABO CENTRUM MEDISCHE GENETICA Dr. Sonia van Dooren, labo-coö ... › doc › het-br...
High incidence of the CFTR mutations A→G and ...
doc.anet.be
by K Storm · · Cited by 9 — Martine Biervliet a. , Lutgardis Van Schil c. ,. Kristine Desager b. , Markus M. Nöthen a,1 a Department of Medical Genetics, University and ... › docman › docman
Improved Splice Site Detection in Genie - Mary Ann Liebert, Inc.
www.liebertpub.com
Syx, Sanne D'hondt, Martine Biervliet, Julie De Backer, Eckhard P. Witten, Sergey Leikin, Elena Makareeva, Gabriele. Gillessen-Kaesbach, Ann Huysseune, ... › pdfplus › cmb
JCS Newsletter 日本循環器学会ニュースメール
www.j-circ.or.jp
... Dominic A.M.J. Theuns, Steven Droogmans, Guy Van Camp, Caroline Weytjens, Martine Biervliet, Maryse Bonduelle, Sonia Van Dooren, Pedro Brugada ... › backnumber
Ledenlijst. Titel Voornaam Naam Discipline Adres Postcode ...
docplayer.info
... Anesthesist i.o. Moorselbaan Aalst Dokter Martine BIERVLIET Huisarts Sint-Gabriëlstraat Liedekerke Dokter Geert BIESEMANS Dermatoloog Leopoldlaan Aalst ... › L...
New ZMPSTE24 (FACE1) mutations in patients HAL-Inserm
www.hal.inserm.fr
by C Navarro · · Cited by 51 — ... David J Amor 10 Kristina Lagerstedt 11Martine Biervliet 12 Peter C van den Akker 13 Pierre Cau 2 Patrice Roll 1, 2, 14 Nicolas Lévy 15, ... › hal
New ZMPSTE24 (FACE1) mutations in patients affected with ...
research.rug.nl
by CL Navarro · · Cited by 51 — ... Martine Biervliet, Peter C. van den Akker, Pierre Cau, Patrice Roll, Nicolas Levy, Catherine Badens, Manfred Wehnert, Annachiara De Sandre-Giovannoli. › publications › new-zmpste24-fa...
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