Devriendt K - Search Results

1

Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes.

Froyen G, Van Esch H, Bauters M, Hollanders K, Frints SG, Vermeesch JR, Devriendt K, Fryns JP, Marynen P. Froyen G, et al. Among authors: devriendt k. Hum Mutat. 2007 Oct;28(10):1034-42. doi: 10.1002/humu.20564. Hum Mutat. 2007. PMID: 17546640

2

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

3

Mosaic trisomy 8 as a cause of velopharyngeal insufficiency.

Vantrappen G, Rommel N, Cremers CW, Fryns JP, Devriendt K. Vantrappen G, et al. Among authors: devriendt k. Am J Med Genet. 2002 Apr 1;108(4):337-8. doi: 10.1002/ajmg.10270. Am J Med Genet. 2002. PMID: 11920842 No abstract available.

4

Atypical presentation of the Prader-Willi syndrome. Mosaic trisomy 15?

Vogels A, Holvoet M, Descheemaeker MJ, Fryns JP, Devriendt K. Vogels A, et al. Among authors: devriendt k. Ann Genet. 2002 Jan-Mar;45(1):1-3. doi: 10.1016/s0003-3995(02)01107-3. Ann Genet. 2002. PMID: 11934381

5

Progressive AV-block and anomalous venous return among cardiac anomalies associated with two novel missense mutations in the CSX/NKX2-5 gene.

Gutierrez-Roelens I, Sluysmans T, Gewillig M, Devriendt K, Vikkula M. Gutierrez-Roelens I, et al. Among authors: devriendt k. Hum Mutat. 2002 Jul;20(1):75-6. doi: 10.1002/humu.9041. Hum Mutat. 2002. PMID: 12112663

6

Somatic mosaicism and variable expression of Townes-Brocks syndrome.

Devriendt K, Fryns JP, Lemmens F, Kohlhase J, Liebers M. Devriendt K, et al. Am J Med Genet. 2002 Aug 1;111(2):230-1. doi: 10.1002/ajmg.10485. Am J Med Genet. 2002. PMID: 12210359 No abstract available.

7

FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation.

De Baere E, Beysen D, Oley C, Lorenz B, Cocquet J, De Sutter P, Devriendt K, Dixon M, Fellous M, Fryns JP, Garza A, Jonsrud C, Koivisto PA, Krause A, Leroy BP, Meire F, Plomp A, Van Maldergem L, De Paepe A, Veitia R, Messiaen L. De Baere E, et al. Among authors: devriendt k. Am J Hum Genet. 2003 Feb;72(2):478-87. doi: 10.1086/346118. Epub 2003 Jan 14. Am J Hum Genet. 2003. PMID: 12529855 Free PMC article.

8

Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: clinical study and mutation analysis of the NXF5 gene.

Frints SG, Jun L, Fryns JP, Devriendt K, Teulingkx R, Van den Berghe L, De Vos B, Borghgraef M, Chelly J, Des Portes V, Van Bokhoven H, Hamel B, Ropers HH, Kalscheuer V, Raynaud M, Moraine C, Marynen P, Froyen G. Frints SG, et al. Among authors: devriendt k. Am J Med Genet A. 2003 Jun 15;119A(3):367-74. doi: 10.1002/ajmg.a.20195. Am J Med Genet A. 2003. PMID: 12784308

9

Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders.

Vogels A, Van Den Ende J, Keymolen K, Mortier G, Devriendt K, Legius E, Fryns JP. Vogels A, et al. Among authors: devriendt k. Eur J Hum Genet. 2004 Mar;12(3):238-40. doi: 10.1038/sj.ejhg.5201135. Eur J Hum Genet. 2004. PMID: 14679397

10

Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.

Castermans D, Wilquet V, Steyaert J, Van de Ven W, Fryns JP, Devriendt K. Castermans D, et al. Among authors: devriendt k. Autism. 2004 Jun;8(2):141-61. doi: 10.1177/1362361304042719. Autism. 2004. PMID: 15165431 Review.

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