Devriendt K - Search Results

1

Partial DiGeorge syndrome in two patients with a 10p rearrangement.

Van Esch H, Groenen P, Daw S, Poffyn A, Holvoet M, Scambler P, Fryns JP, Van de Ven W, Devriendt K. Van Esch H, et al. Among authors: devriendt k. Clin Genet. 1999 Apr;55(4):269-76. doi: 10.1034/j.1399-0004.1999.550410.x. Clin Genet. 1999. PMID: 10361989

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

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.

4

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.

5

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

6

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.

7

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

8

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

9

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

10

Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndrome.

Devriendt K, D'Espallier L, Fryns JP. Devriendt K, et al. J Med Genet. 1996 Mar;33(3):224-6. doi: 10.1136/jmg.33.3.224. J Med Genet. 1996. PMID: 8728696 Free PMC article.

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