Devriendt K - Search Results

1

Comprehensive genome-wide analysis of routine non-invasive test data allows cancer prediction: A single-center retrospective analysis of over 85,000 pregnancies.

Lenaerts L, Brison N, Maggen C, Vancoillie L, Che H, Vandenberghe P, Dierickx D, Michaux L, Dewaele B, Neven P, Floris G, Tousseyn T, Lannoo L, Jatsenko T, Bempt IV, Van Calsteren K, Vandecaveye V, Dehaspe L, Devriendt K, Legius E, Bogaert KVD, Vermeesch JR, Amant F. Lenaerts L, et al. Among authors: devriendt k. EClinicalMedicine. 2021 May 13;35:100856. doi: 10.1016/j.eclinm.2021.100856. eCollection 2021 May. EClinicalMedicine. 2021. PMID: 34036251 Free PMC article.

2

Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome?

Devriendt K, Legius E, Fryns JP. Devriendt K, et al. Am J Med Genet. 1996 Mar 1;62(1):54-7. doi: 10.1002/(SICI)1096-8628(19960301)62:1<54::AID-AJMG11>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8779325

3

Cohen syndrome: the clinical symptoms and stigmata at a young age.

Fryns JP, Legius E, Devriendt K, Meire F, Standaert L, Baten E, Van den Berghe H. Fryns JP, et al. Among authors: devriendt k. Clin Genet. 1996 May;49(5):237-41. doi: 10.1111/j.1399-0004.1996.tb03780.x. Clin Genet. 1996. PMID: 8832131

4

Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.

Devriendt K, Matthijs G, Claes S, Legius E, Proesmans W, Cassiman JJ, Fryns JP. Devriendt K, et al. J Med Genet. 1997 Apr;34(4):318-22. doi: 10.1136/jmg.34.4.318. J Med Genet. 1997. PMID: 9138157 Free PMC article.

5

Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.

Devriendt K, Petit P, Matthijs G, Vermeesch JR, Holvoet M, De Muelenaere A, Marynen P, Cassiman JJ, Fryns JP. Devriendt K, et al. J Med Genet. 1997 May;34(5):395-9. doi: 10.1136/jmg.34.5.395. J Med Genet. 1997. PMID: 9152837 Free PMC article.

6

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

Swillen A, Devriendt K, Legius E, Eyskens B, Dumoulin M, Gewillig M, Fryns JP. Swillen A, et al. Among authors: devriendt k. J Med Genet. 1997 Jun;34(6):453-8. doi: 10.1136/jmg.34.6.453. J Med Genet. 1997. PMID: 9192263 Free PMC article.

7

Two adult females with a distinct familial mental retardation syndrome: non-progressive neurological symptoms with ataxia and hypotonia, similar facial appearance, hypergonadotrophic hypogonadism, and retinal dystrophy.

Fryns JP, Van Lingen C, Devriendt K, Legius E, Raus P. Fryns JP, et al. Among authors: devriendt k. J Med Genet. 1998 Apr;35(4):333-5. doi: 10.1136/jmg.35.4.333. J Med Genet. 1998. PMID: 9598731 Free PMC article.

8

Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation.

Petit P, Devriendt K, Vermeesch JR, De Cock P, Fryns JP. Petit P, et al. Among authors: devriendt k. Ann Genet. 1998;41(1):22-6. Ann Genet. 1998. PMID: 9599647

9

Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).

Petit P, Devriendt K, Vermeesch JR, Meireleire J, Fryns JP. Petit P, et al. Among authors: devriendt k. Genet Couns. 1998;9(3):215-21. Genet Couns. 1998. PMID: 9777345

10

The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescents.

Vogels A, Devriendt K, Legius E, Decock P, Marien J, Hendrickx G, Fryns JP. Vogels A, et al. Among authors: devriendt k. Genet Couns. 1998;9(4):245-53. Genet Couns. 1998. PMID: 9894160

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