Devriendt K - Search Results

1

The C20orf133 gene is disrupted in a patient with Kabuki syndrome.

Maas NM, Van de Putte T, Melotte C, Francis A, Schrander-Stumpel CT, Sanlaville D, Genevieve D, Lyonnet S, Dimitrov B, Devriendt K, Fryns JP, Vermeesch JR. Maas NM, et al. Among authors: devriendt k. J Med Genet. 2007 Sep;44(9):562-9. doi: 10.1136/jmg.2007.049510. Epub 2007 Jun 23. J Med Genet. 2007. PMID: 17586838 Free PMC article.

2

Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome. Construction of a mouse-human hybrid cell line containing an i(12p) as the sole human chromosome.

Zhang J, Marynen P, Devriendt K, Fryns JP, Van den Berghe H, Cassiman JJ. Zhang J, et al. Among authors: devriendt k. Hum Genet. 1989 Nov;83(4):359-63. doi: 10.1007/BF00291381. Hum Genet. 1989. PMID: 2807276

3

Diaphragmatic hernia in Denys-Drash syndrome.

Devriendt K, Deloof E, Moerman P, Legius E, Vanhole C, de Zegher F, Proesmans W, Devlieger H. Devriendt K, et al. Am J Med Genet. 1995 May 22;57(1):97-101. doi: 10.1002/ajmg.1320570120. Am J Med Genet. 1995. PMID: 7645607

4

Hydrocephalus with features of VATER.

Devriendt K, De Cock P, Fryns JP. Devriendt K, et al. Genet Couns. 1995;6(1):69. Genet Couns. 1995. PMID: 7794566 Review. No abstract available.

5

The Kabuki make-up (Niikawa-Kuroki) syndrome and isolated transient hyperphosphatasemia.

Devriendt K, Fryns JP. Devriendt K, et al. Clin Genet. 1994 Jun;45(6):330-1. doi: 10.1111/j.1399-0004.1994.tb04043.x. Clin Genet. 1994. PMID: 7923866 No abstract available.

6

Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p.

Fryns JP, Kleczkowska A, Devriendt K, Devliegher H, Van den Berghe H. Fryns JP, et al. Among authors: devriendt k. Genet Couns. 1993;4(1):37-41. Genet Couns. 1993. PMID: 8471219

7

Genetic locus on chromosome 6p for multicystic renal dysplasia, pelvi-ureteral junction stenosis, and vesicoureteral reflux.

Devriendt K, Fryns JP. Devriendt K, et al. Am J Med Genet. 1995 Nov 20;59(3):396-8. doi: 10.1002/ajmg.1320590326. Am J Med Genet. 1995. PMID: 8599371 No abstract available.

8

Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndrome.

Devriendt K, De Mars K, De Cock P, Gewillig M, Fryns JP. Devriendt K, et al. Ann Genet. 1995;38(4):228-30. Ann Genet. 1995. PMID: 8629811

9

Ichthyosis-characteristic appearance-mental retardation syndrome with distinct histological skin abnormalities.

Devriendt K, van den Oord J, De Vos R, Van den Berghe H, Fryns JP. Devriendt K, et al. Am J Med Genet. 1996 Jan 11;61(2):127-30. doi: 10.1002/(SICI)1096-8628(19960111)61:2<127::AID-AJMG4>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8669437

10

Alopecia-mental retardation syndrome associated with convulsions and hypergonadotropic hypogonadism.

Devriendt K, Van den Berghe H, Fryns JP. Devriendt K, et al. Clin Genet. 1996 Jan;49(1):6-9. doi: 10.1111/j.1399-0004.1996.tb04316.x. Clin Genet. 1996. PMID: 8721564

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