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598 results

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Page 1
SPG20 mutation in three siblings with familial hereditary spastic paraplegia.
Dardour L, Roelens F, Race V, Souche E, Holvoet M, Devriendt K. Dardour L, et al. Among authors: devriendt k. Cold Spring Harb Mol Case Stud. 2017 Jul 5;3(4):a001537. doi: 10.1101/mcs.a001537. Print 2017 Jul. Cold Spring Harb Mol Case Stud. 2017. PMID: 28679690 Free PMC article.
Glypican 1 gene: good candidate for brachydactyly type E.
Syrrou M, Keymolen K, Devriendt K, Holvoet M, Thoelen R, Verhofstadt K, Fryns JP. Syrrou M, et al. Among authors: devriendt k. Am J Med Genet. 2002 Apr 1;108(4):310-4. doi: 10.1002/ajmg.10266. Am J Med Genet. 2002. PMID: 11920836
Novel TBX5 mutations in patients with Holt-Oram syndrome.
Debeer P, Race V, Gewillig M, Devriendt K, Frijns JP. Debeer P, et al. Among authors: devriendt k. Clin Orthop Relat Res. 2007 Sep;462:20-6. doi: 10.1097/BLO.0b013e3181123ffe. Clin Orthop Relat Res. 2007. PMID: 17534187
The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability.
Vandewalle J, Bauters M, Van Esch H, Belet S, Verbeeck J, Fieremans N, Holvoet M, Vento J, Spreiz A, Kotzot D, Haberlandt E, Rosenfeld J, Andrieux J, Delobel B, Dehouck MB, Devriendt K, Fryns JP, Marynen P, Goldstein A, Froyen G. Vandewalle J, et al. Among authors: devriendt k. Hum Genet. 2013 Oct;132(10):1177-85. doi: 10.1007/s00439-013-1322-3. Epub 2013 Jun 20. Hum Genet. 2013. PMID: 23783460
Pseudoautosomal region 1 length polymorphism in the human population.
Mensah MA, Hestand MS, Larmuseau MH, Isrie M, Vanderheyden N, Declercq M, Souche EL, Van Houdt J, Stoeva R, Van Esch H, Devriendt K, Voet T, Decorte R, Robinson PN, Vermeesch JR. Mensah MA, et al. Among authors: devriendt k. PLoS Genet. 2014 Nov 6;10(11):e1004578. doi: 10.1371/journal.pgen.1004578. eCollection 2014 Nov. PLoS Genet. 2014. PMID: 25375121 Free PMC article.
Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing.
Brison N, Neofytou M, Dehaspe L, Bayindir B, Van Den Bogaert K, Dardour L, Peeters H, Van Esch H, Van Buggenhout G, Vogels A, de Ravel T, Legius E, Devriendt K, Vermeesch JR. Brison N, et al. Among authors: devriendt k. Prenat Diagn. 2018 Mar;38(4):258-266. doi: 10.1002/pd.5223. Epub 2018 Feb 19. Prenat Diagn. 2018. PMID: 29388226
598 results