Devriendt K - Search Results

1

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

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

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

9

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.

10

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.

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