Willems PJ - Search Results

1

Assignment of the human integral transmembrane protein 1 gene (ITM1) to human chromosome band 11q23.3 by in situ hybridization and YAC mapping.

Van Hul W, Hong G, Wauters J, Van Hul E, Nowak N, Shows TB, Willems PJ, Merregaert J. Van Hul W, et al. Among authors: willems pj. Cytogenet Cell Genet. 1996;74(3):218-9. doi: 10.1159/000134417. Cytogenet Cell Genet. 1996. PMID: 8941377 No abstract available.

2

Regional mapping of a liver alpha-subunit gene of phosphorylase kinase (PHKA) to the distal region of human chromosome Xp.

Wauters JG, Bossuyt PJ, Davidson J, Hendrickx J, Kilimann MW, Willems PJ. Wauters JG, et al. Among authors: willems pj. Cytogenet Cell Genet. 1992;60(3-4):194-6. doi: 10.1159/000133334. Cytogenet Cell Genet. 1992. PMID: 1505214

3

Refined physical mapping and genomic structure of the EXTL1 gene.

Wuyts W, Spieker N, Van Roy N, De Boulle K, De Paepe A, Willems PJ, Van Hul W, Versteeg R, Speleman F. Wuyts W, et al. Among authors: willems pj. Cytogenet Cell Genet. 1999;86(3-4):267-70. doi: 10.1159/000015317. Cytogenet Cell Genet. 1999. PMID: 10575224

4

Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST).

Balemans W, Ebeling M, Patel N, Van Hul E, Olson P, Dioszegi M, Lacza C, Wuyts W, Van Den Ende J, Willems P, Paes-Alves AF, Hill S, Bueno M, Ramos FJ, Tacconi P, Dikkers FG, Stratakis C, Lindpaintner K, Vickery B, Foernzler D, Van Hul W. Balemans W, et al. Hum Mol Genet. 2001 Mar 1;10(5):537-43. doi: 10.1093/hmg/10.5.537. Hum Mol Genet. 2001. PMID: 11181578

5

Positional cloning of a gene involved in hereditary multiple exostoses.

Wuyts W, Van Hul W, Wauters J, Nemtsova M, Reyniers E, Van Hul EV, De Boulle K, de Vries BB, Hendrickx J, Herrygers I, Bossuyt P, Balemans W, Fransen E, Vits L, Coucke P, Nowak NJ, Shows TB, Mallet L, van den Ouweland AM, McGaughran J, Halley DJ, Willems PJ. Wuyts W, et al. Among authors: willems pj. Hum Mol Genet. 1996 Oct;5(10):1547-57. doi: 10.1093/hmg/5.10.1547. Hum Mol Genet. 1996. PMID: 8894688

6

Localization of a gene for autosomal dominant osteopetrosis (Albers-Schönberg disease) to chromosome 1p21.

Van Hul W, Bollerslev J, Gram J, Van Hul E, Wuyts W, Benichou O, Vanhoenacker F, Willems PJ. Van Hul W, et al. Among authors: willems pj. Am J Hum Genet. 1997 Aug;61(2):363-9. doi: 10.1086/514844. Am J Hum Genet. 1997. PMID: 9311741 Free PMC article.

7

Identification and characterization of a novel member of the EXT gene family, EXTL2.

Wuyts W, Van Hul W, Hendrickx J, Speleman F, Wauters J, De Boulle K, Van Roy N, Van Agtmael T, Bossuyt P, Willems PJ. Wuyts W, et al. Among authors: willems pj. Eur J Hum Genet. 1997 Nov-Dec;5(6):382-9. Eur J Hum Genet. 1997. PMID: 9450183

8

Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21.

Van Hul W, Balemans W, Van Hul E, Dikkers FG, Obee H, Stokroos RJ, Hildering P, Vanhoenacker F, Van Camp G, Willems PJ. Van Hul W, et al. Among authors: willems pj. Am J Hum Genet. 1998 Feb;62(2):391-9. doi: 10.1086/301721. Am J Hum Genet. 1998. PMID: 9463328 Free PMC article.

9

Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene family.

Van Hul W, Wuyts W, Hendrickx J, Speleman F, Wauters J, De Boulle K, Van Roy N, Bossuyt P, Willems PJ. Van Hul W, et al. Among authors: willems pj. Genomics. 1998 Jan 15;47(2):230-7. doi: 10.1006/geno.1997.5101. Genomics. 1998. PMID: 9479495

10

Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21.

Balemans W, Van Den Ende J, Freire Paes-Alves A, Dikkers FG, Willems PJ, Vanhoenacker F, de Almeida-Melo N, Alves CF, Stratakis CA, Hill SC, Van Hul W. Balemans W, et al. Among authors: willems pj. Am J Hum Genet. 1999 Jun;64(6):1661-9. doi: 10.1086/302416. Am J Hum Genet. 1999. PMID: 10330353 Free PMC article.

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