Devriendt K - Search Results

1

Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements.

Demaerel W, Hestand MS, Vergaelen E, Swillen A, López-Sánchez M, Pérez-Jurado LA, McDonald-McGinn DM, Zackai E, Emanuel BS, Morrow BE, Breckpot J, Devriendt K, Vermeesch JR; International 22q11.2 Brain and Behavior Consortium. Demaerel W, et al. Among authors: devriendt k. Am J Hum Genet. 2017 Oct 5;101(4):616-622. doi: 10.1016/j.ajhg.2017.09.002. Epub 2017 Sep 28. Am J Hum Genet. 2017. Retraction in: Am J Hum Genet. 2018 Sep 6;103(3):457. doi: 10.1016/j.ajhg.2018.08.011. PMID: 28965848 Free PMC article. Retracted.

2

Loss of the Y-chromosome in a malignant Sertoli tumor.

Aly MS, Dal Cin P, Moerman P, De Wever I, Devriendt K, Brock P, Casteels-Van Daele M, Van den Berghe H. Aly MS, et al. Among authors: devriendt k. Cancer Genet Cytogenet. 1993 Feb;65(2):104-6. doi: 10.1016/0165-4608(93)90215-8. Cancer Genet Cytogenet. 1993. PMID: 8453593 No abstract available.

3

Renal and urological tract malformations caused by a 22q11 deletion.

Devriendt K, Swillen A, Fryns JP, Proesmans W, Gewillig M. Devriendt K, et al. J Med Genet. 1996 Apr;33(4):349. doi: 10.1136/jmg.33.4.349. J Med Genet. 1996. PMID: 8730297 Free PMC article. No abstract available.

4

Cerebellar hypoplasia in a patient with velo-cardio-facial syndrome.

Devriendt K, Thienen MN, Swillen A, Fryns JP. Devriendt K, et al. Dev Med Child Neurol. 1996 Oct;38(10):949-53. doi: 10.1111/j.1469-8749.1996.tb15052.x. Dev Med Child Neurol. 1996. PMID: 8870617

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

Chromosome 22q11 deletion presenting as the Potter sequence.

Devriendt K, Moerman P, Van Schoubroeck D, Vandenberghe K, Fryns JP. Devriendt K, et al. J Med Genet. 1997 May;34(5):423-5. doi: 10.1136/jmg.34.5.423. J Med Genet. 1997. PMID: 9152843 Free PMC article.

7

Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletion.

Devriendt K, Van Hoestenberghe R, Van Hole C, Devlieger H, Gewillig M, Moerman P, Van den Berghe H, Fryns JP. Devriendt K, et al. Clin Genet. 1997 Apr;51(4):246-9. doi: 10.1111/j.1399-0004.1997.tb02463.x. Clin Genet. 1997. PMID: 9184246

8

Interstitial telomeric sequences at the junction site of a jumping translocation.

Vermeesch JR, Petit P, Speleman F, Devriendt K, Fryns JP, Marynen P. Vermeesch JR, et al. Among authors: devriendt k. Hum Genet. 1997 Jun;99(6):735-7. doi: 10.1007/s004390050440. Hum Genet. 1997. PMID: 9187665

9

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.

10

Polyhydramnios as a prenatal symptom of the digeorge/velo-cardio-facial syndrome.

Devriendt K, Van Schoubroeck D, Eyskens B, Vantrappen G, Swillen A, Gewillig M, Dumoulin M, Moerman P, Vandenberghe K, Fryns JP. Devriendt K, et al. Prenat Diagn. 1998 Jan;18(1):68-72. Prenat Diagn. 1998. PMID: 9483643

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