مقالههای دارای تعهدات انتشار عمومی - Mustapha Amyereبیشتر بدانید
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Chromosome instability is common in human cleavage-stage embryos
E Vanneste, T Voet, C Le Caignec, M Ampe, P Konings, C Melotte, ...
Nature medicine 15 (5), 577, 2009
تعهدات: Research Foundation (Flanders)
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis
B Lorenz-Depiereux, M Bastepe, A Benet-Pagès, M Amyere, ...
Nature genetics 38 (11), 1248-1250, 2006
تعهدات: German Research Foundation
Germline loss-of-function mutations in EPHB4 cause a second form of capillary malformation-arteriovenous malformation (CM-AVM2) deregulating RAS-MAPK signaling
M Amyere, N Revencu, R Helaers, E Pairet, E Baselga, M Cordisco, ...
Circulation 136 (11), 1037-1048, 2017
تعهدات: US National Institutes of Health, National Fund for Scientific Research, Belgium
TMEM165 deficiency causes a congenital disorder of glycosylation
F Foulquier, M Amyere, J Jaeken, R Zeevaert, E Schollen, V Race, ...
The American Journal of Human Genetics 91 (1), 15-26, 2012
تعهدات: US National Institutes of Health, Research Foundation (Flanders)
Somatic uniparental isodisomy explains multifocality of glomuvenous malformations
M Amyere, V Aerts, P Brouillard, BAS McIntyre, FP Duhoux, M Wassef, ...
The American Journal of Human Genetics 92 (2), 188-196, 2013
تعهدات: US National Institutes of Health
Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16
I Balikova, K Martens, C Melotte, M Amyere, S Van Vooren, Y Moreau, ...
The American Journal of Human Genetics 82 (1), 181-187, 2008
تعهدات: Research Foundation (Flanders)
Common somatic alterations identified in maffucci syndrome by molecular karyotyping
M Amyere, A Dompmartin, V Wouters, O Enjolras, I Kaitila, PL Docquier, ...
Molecular syndromology 5 (6), 259-267, 2014
تعهدات: US National Institutes of Health, National Fund for Scientific Research, Belgium
Giant cell tumor occurring in familial Paget's disease of bone: report of clinical characteristics and linkage analysis of a large pedigree
F Gianfrancesco, D Rendina, D Merlotti, T Esposito, M Amyere, ...
Journal of Bone and Mineral Research 28 (2), 341-350, 2013
تعهدات: Fondazione Telethon, Italy
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