受强制性开放获取政策约束的文章 - devriendt了解详情
无法在其他位置公开访问的文章：24 篇
A balanced translocation t (6; 14)(q25. 3; q13. 2) leading to reciprocal fusion transcripts in a patient with intellectual disability and agenesis of corpus callosum
L Backx, E Seuntjens, K Devriendt, J Vermeesch, H Van Esch
Cytogenetic and genome research 132 (3), 135-143, 2010
强制性开放获取政策： Research Foundation (Flanders)
Narrowing the critical deletion region for autism spectrum disorders on 16p11. 2.
A Crepel, J Steyaert, W De la Marche, V De Wolf, JP Fryns, I Noens, ...
American journal of medical genetics. Part B, Neuropsychiatric genetics: the …, 2011
强制性开放获取政策： Research Foundation (Flanders)
Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic congenital diaphragmatic hernia
PD Brady, P Moerman, L De Catte, J Deprest, K Devriendt, JR Vermeesch
European Journal of Medical Genetics 57 (9), 487-493, 2014
强制性开放获取政策： Research Foundation (Flanders), European Commission
Identification of dosage‐sensitive genes in fetuses referred with severe isolated congenital diaphragmatic hernia
PD Brady, P DeKoninck, JP Fryns, K Devriendt, JA Deprest, ...
Prenatal diagnosis 33 (13), 1283-1292, 2013
强制性开放获取政策： Research Foundation (Flanders), European Commission
Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next‐generation sequencing
M Kammoun, E Souche, P Brady, J Ding, N Cosemans, E Gratacos, ...
Prenatal Diagnosis 38 (9), 654-663, 2018
强制性开放获取政策： Government of Spain, Belgian Science Policy Office
Haploinsufficiency of the gene Quaking (QKI) is associated with the 6q terminal deletion syndrome
L Backx, JP Fryns, C Marcelis, K Devriendt, J Vermeesch, H Van Esch
American Journal of Medical Genetics Part A 152 (2), 319-326, 2010
强制性开放获取政策： Research Foundation (Flanders)
Novel TBX5 mutations in patients with Holt-Oram syndrome
P Debeer, V Race, M Gewillig, K Devriendt, JP Frijns
Clinical Orthopaedics and Related Research® 462, 20-26, 2007
强制性开放获取政策： Research Foundation (Flanders)
Sporadic male patients with intellectual disability: contribution of X-chromosome copy number variants
M Isrie, G Froyen, K Devriendt, T De Ravel, JP Fryns, JR Vermeesch, ...
European journal of medical genetics 55 (11), 577-585, 2012
强制性开放获取政策： Research Foundation (Flanders)
Cell-free DNA methylome analysis for early preeclampsia prediction
M De Borre, H Che, Q Yu, L Lannoo, K De Ridder, L Vancoillie, ...
Nature Medicine 29 (9), 2206-2215, 2023
强制性开放获取政策： Research Foundation (Flanders)
The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability
J Vandewalle, M Bauters, H Van Esch, S Belet, J Verbeeck, N Fieremans, ...
Human genetics 132, 1177-1185, 2013
强制性开放获取政策： Research Foundation (Flanders)
A new approach to imprinting mutation detection in GNAS by Sequenom EpiTYPER system
B Izzi, B Decallonne, K Devriendt, R Bouillon, D Vanderschueren, ...
Clinica Chimica Acta 411 (23-24), 2033-2039, 2010
强制性开放获取政策： Research Foundation (Flanders)
Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndrome
E Loos, N Verhaert, A Willaert, K Devriendt, A Swillen, R Hermans, ...
American Journal of Medical Genetics Part A 170 (11), 2975-2983, 2016
强制性开放获取政策： Research Foundation (Flanders)
Isolated terminal limb reduction defects: Extending the clinical spectrum of Adams–Oliver syndrome and ARHGAP31 mutations
M Isrie, W Wuyts, H Van Esch, K Devriendt
American Journal of Medical Genetics Part A 164 (6), 1576-1579, 2014
强制性开放获取政策： Research Foundation (Flanders)
Array-based approaches in prenatal diagnosis
PD Brady, K Devriendt, J Deprest, JR Vermeesch
Genomic Structural Variants: Methods and Protocols, 151-171, 2012
强制性开放获取政策： Research Foundation (Flanders)
High frequency of submicroscopic chromosomal deletions in patients with idiopathic congenital eye malformations
I Balikova, T de Ravel, C Ayuso, B Thienpont, I Casteels, C Villaverde, ...
American journal of ophthalmology 151 (6), 1087-1094. e45, 2011
强制性开放获取政策： Research Foundation (Flanders), Government of Spain
Non‐invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?
L Lannoo, L Lenaerts, K Van Den Bogaert, H Che, N Brison, K Devriendt, ...
Prenatal diagnosis 41 (10), 1264-1272, 2021
强制性开放获取政策： Research Foundation (Flanders)
Exome sequencing identifies ZFPM2 as a cause of familial isolated congenital diaphragmatic hernia and possibly cardiovascular malformations
PD Brady, J Van Houdt, B Callewaert, J Deprest, K Devriendt, ...
European journal of medical genetics 57 (6), 247-252, 2014
强制性开放获取政策： Research Foundation (Flanders), European Commission
Genotypic and phenotypic variation in six patients with solitary median maxillary central incisor syndrome
S Poelmans, T Kawamoto, F Cristofoli, C Politis, J Vermeesch, ...
American Journal of Medical Genetics Part A 167 (10), 2451-2458, 2015
强制性开放获取政策： Research Foundation (Flanders)
A complex Xp11.22 deletion in a patient with syndromic autism: Exploration of FAM120C as a positional candidate gene for autism
V De Wolf, A Crepel, F Schuit, L van Lommel, B Ceulemans, J Steyaert, ...
American journal of medical genetics Part A 164 (12), 3035-3041, 2014
强制性开放获取政策： Research Foundation (Flanders)
Duplication of the TGFBR1 gene causes features of Loeys-Dietz syndrome
J Breckpot, W Budts, F De Zegher, JR Vermeesch, K Devriendt
European Journal of Medical Genetics 53 (6), 408-410, 2010
强制性开放获取政策： Research Foundation (Flanders)
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