C. Huysmans

发表

Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD).

K. Devriendt, H. Van Esch, W. V. D. Van de Ven, 2005, European journal of medical genetics.

Transcriptional control of the human high mobility group A1 gene: basal and oncogenic Ras-regulated expression.

W. V. D. Van de Ven, I. Cleynen, S. Shirasawa, 2007, Cancer research.

Allelic knockout of novel splice variants of human recombination repair gene RAD51B in t(12;14) uterine leiomyomas.

W. V. D. Van de Ven, E. Schoenmakers, C. Huysmans, 1999, Cancer research.

PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse

H. Peeters, N. Niikawa, A. Bairoch, 2003, Human Genetics.

Mapping of the translocation breakpoints of primary pleomorphic adenomas and lipomas within a common region of chromosome 12.

W. V. D. Van de Ven, J. Bullerdiek, E. Schoenmakers, 1996, Cancer genetics and cytogenetics.

Mapping of the gene encoding the human hepatoma-derived growth factor (HDGF) with homology to the high-mobility group (HMG)-1 protein to Xq25.

W. V. D. Van de Ven, J. Bullerdiek, E. Schoenmakers, 1996, Genomics.

LHFP, a novel translocation partner gene of HMGIC in a lipoma, is a member of a new family of LHFP-like genes.

W. V. D. Van de Ven, N. Mandahl, E. Schoenmakers, 1999, Genomics.

Involvement of a palindromic chromosome 22‐specific low‐copy repeat in a constitutional t(X; 22)(q27;q11)

K. Devriendt, J. Fryns, R. Mols, 2002, Clinical genetics.

A 6-Mb yeast artificial chromosome contig and long-range physical map encompassing the region on chromosome 12q15 frequently rearranged in a variety of benign solid tumors.

W. V. D. Van de Ven, J. Bullerdiek, E. Schoenmakers, 1995, Genomics.

The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism

K. Devriendt, J. Steyaert, W. V. D. Van de Ven, 2003, Journal of medical genetics.

Advances in Brief Allelic Knockout of Novel Splice Variants of Human Recombination Repair Gene RAD 51 B in t ( 12 ; 14 ) Uterine Leiomyomas 1

E. Schoenmakers, C. Huysmans, W. V. D. Ven, 1998 .

Carpal and tarsal synostoses and transverse reduction defects of the toes in two brothers heterozygous for a double de novo NOGGIN mutation

K. Devriendt, W. V. D. Van de Ven, J. Fryns, 2005, American journal of medical genetics. Part A.

A novel NOG mutation Pro37Arg in a family with tarsal and carpal synostoses

K. Devriendt, W. V. D. Van de Ven, J. Fryns, 2004, American journal of medical genetics. Part A.

Poster session 2

Hugo A. Katus, V. V. Miroshnikova, Paolo Dario, 2004, EP Europace.

Human homologues of Osr1 and Osr2 are not involved in a syndrome with distal limb deficiencies, oral abnormalities, and renal defects.

T. de Ravel, K. Devriendt, W. V. D. Van de Ven, 2002, American journal of medical genetics.

Mapping of the human HMG2 gene to 4q31.

W. V. D. Van de Ven, E. Schoenmakers, S. Bartnitzke, 1996, Genomics.