Van Hul W - Search Results

1

Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11.

Wuyts W, Ramlakhan S, Van Hul W, Hecht JT, van den Ouweland AM, Raskind WH, Hofstede FC, Reyniers E, Wells DE, de Vries B, et al. Wuyts W, et al. Among authors: van den ouweland am, van hul w. Am J Hum Genet. 1995 Aug;57(2):382-7. Am J Hum Genet. 1995. PMID: 7668264 Free PMC article.

2

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication.

Timmerman V, Nelis E, Van Hul W, Nieuwenhuijsen BW, Chen KL, Wang S, Ben Othman K, Cullen B, Leach RJ, Hanemann CO, et al. Timmerman V, et al. Among authors: van hul w. Nat Genet. 1992 Jun;1(3):171-5. doi: 10.1038/ng0692-171. Nat Genet. 1992. PMID: 1303230

3

Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.

Raeymaekers P, Timmerman V, Nelis E, Van Hul W, De Jonghe P, Martin JJ, Van Broeckhoven C. Raeymaekers P, et al. Among authors: van broeckhoven c, van hul w. J Med Genet. 1992 Jan;29(1):5-11. doi: 10.1136/jmg.29.1.5. J Med Genet. 1992. PMID: 1552545 Free PMC article.

4

DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type).

Bakker E, van Broeckhoven C, Haan J, Voorhoeve E, van Hul W, Levy E, Lieberburg I, Carman MD, van Ommen GJ, Frangione B, et al. Bakker E, et al. Among authors: van ommen gj, van broeckhoven c, van hul w. Am J Hum Genet. 1991 Sep;49(3):518-21. Am J Hum Genet. 1991. PMID: 1679289 Free PMC article.

5

Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome.

Van Camp G, Backhovens H, Cruts M, Wehnert A, Van Hul W, Stinissen P, Van Broeckhoven C. Van Camp G, et al. Among authors: van broeckhoven c, van hul w. Hum Genet. 1991 Oct;87(6):649-53. doi: 10.1007/BF00201718. Hum Genet. 1991. PMID: 1682232

6

Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybrids.

Van Camp G, Van Hul W, Backhovens H, Stinissen P, Wehnert A, Patterson D, Vandenberghe A, Van Broeckhoven C. Van Camp G, et al. Among authors: van broeckhoven c, van hul w. Somat Cell Mol Genet. 1990 May;16(3):241-9. doi: 10.1007/BF01233360. Somat Cell Mol Genet. 1990. PMID: 1972817

7

Subregional localization of the chromosome 21 loci D21S24 and D21S26 using physical mapping techniques.

Van Hul W, Backhovens H, Van Camp G, Stinissen P, Cruts M, Wehnert A, Van Broeckhoven C. Van Hul W, et al. Among authors: van broeckhoven c, van camp g. Hum Genet. 1991 Jun;87(2):109-11. doi: 10.1007/BF00204162. Hum Genet. 1991. PMID: 2066096

8

Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndrome.

Van Camp G, Stinissen P, Van Hul W, Backhovens H, Wehnert A, Vandenberge A, Van Broeckhoven C. Van Camp G, et al. Among authors: van broeckhoven c, van hul w. Hum Genet. 1989 Aug;83(1):58-60. doi: 10.1007/BF00274149. Hum Genet. 1989. PMID: 2570018

9

Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.

Bartsch O, Wuyts W, Van Hul W, Hecht JT, Meinecke P, Hogue D, Werner W, Zabel B, Hinkel GK, Powell CM, Shaffer LG, Willems PJ. Bartsch O, et al. Among authors: van hul w. Am J Hum Genet. 1996 Apr;58(4):734-42. Am J Hum Genet. 1996. PMID: 8644736 Free PMC article.

10

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: van hul ev, van den ouweland am, van hul w. Hum Mol Genet. 1996 Oct;5(10):1547-57. doi: 10.1093/hmg/5.10.1547. Hum Mol Genet. 1996. PMID: 8894688

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