Devriendt K - Search Results

1

Novel PORCN mutations in focal dermal hypoplasia.

Froyen G, Govaerts K, Van Esch H, Verbeeck J, Tuomi ML, Heikkilä H, Torniainen S, Devriendt K, Fryns JP, Marynen P, Järvelä I, Ala-Mello S. Froyen G, et al. Among authors: devriendt k. Clin Genet. 2009 Dec;76(6):535-43. doi: 10.1111/j.1399-0004.2009.01248.x. Epub 2009 Oct 23. Clin Genet. 2009. PMID: 19863546

2

Structure of the human alpha-2 macroglobulin gene and its promotor.

Matthijs G, Devriendt K, Cassiman JJ, Van den Berghe H, Marynen P. Matthijs G, et al. Among authors: devriendt k. Biochem Biophys Res Commun. 1992 Apr 30;184(2):596-603. doi: 10.1016/0006-291x(92)90631-t. Biochem Biophys Res Commun. 1992. PMID: 1374237

3

A genetic polymorphism in a functional domain of human pregnancy zone protein: the bait region. Genomic structure of the bait domains of human pregnancy zone protein and alpha 2 macroglobulin.

Marynen P, Devriendt K, Van den Berghe H, Cassiman JJ. Marynen P, et al. Among authors: devriendt k. FEBS Lett. 1990 Mar 26;262(2):349-52. doi: 10.1016/0014-5793(90)80226-9. FEBS Lett. 1990. PMID: 1692292 Free article.

4

Primary structure of pregnancy zone protein. Molecular cloning of a full-length PZP cDNA clone by the polymerase chain reaction.

Devriendt K, Van den Berghe H, Cassiman JJ, Marynen P. Devriendt K, et al. Biochim Biophys Acta. 1991 Jan 17;1088(1):95-103. doi: 10.1016/0167-4781(91)90157-h. Biochim Biophys Acta. 1991. PMID: 1989698

5

Chromosome mapping using polymerase chain reaction on somatic cell hybrids.

Zhang J, Devriendt K, Marynen P, Van den Berghe H, Cassiman JJ. Zhang J, et al. Among authors: devriendt k. Cancer Genet Cytogenet. 1990 Apr;45(2):217-21. doi: 10.1016/0165-4608(90)90085-o. Cancer Genet Cytogenet. 1990. PMID: 2317769

6

A cluster of alpha 2-macroglobulin-related genes (alpha 2 M) on human chromosome 12p: cloning of the pregnancy-zone protein gene and an alpha 2M pseudogene.

Devriendt K, Zhang J, van Leuven F, van den Berghe H, Cassiman JJ, Marynen P. Devriendt K, et al. Gene. 1989 Sep 30;81(2):325-34. doi: 10.1016/0378-1119(89)90193-5. Gene. 1989. PMID: 2478422

7

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

8

Severe alport phenotype in a woman with two missense mutations in the same COL4A5 gene and preponderant inactivation of the X chromosome carrying the normal allele.

Guo C, Van Damme B, Vanrenterghem Y, Devriendt K, Cassiman JJ, Marynen P. Guo C, et al. Among authors: devriendt k. J Clin Invest. 1995 Apr;95(4):1832-7. doi: 10.1172/JCI117862. J Clin Invest. 1995. PMID: 7706490 Free PMC article.

9

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.

10

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

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