Van Hul W - Search Results

1

A contiguous physical map of the pericentromeric region of chromosome 21q between D21Z1 and D21S13E.

Van Hul W, Van Camp G, Stuyver L, Delabar JM, McInnis MG, Warren AC, Antonarakis SE, Van Broeckhoven C. Van Hul W, et al. Among authors: van broeckhoven c, van camp g. Genomics. 1993 Mar;15(3):626-30. doi: 10.1006/geno.1993.1117. Genomics. 1993. PMID: 8468058

2

Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene.

Hendriks L, van Duijn CM, Cras P, Cruts M, Van Hul W, van Harskamp F, Warren A, McInnis MG, Antonarakis SE, Martin JJ, et al. Hendriks L, et al. Among authors: van duijn cm, van harskamp f, van hul w. Nat Genet. 1992 Jun;1(3):218-21. doi: 10.1038/ng0692-218. Nat Genet. 1992. PMID: 1303239

3

D21S215 is a (GT)n polymorphic marker close to centromeric alphoid sequences on chromosome 21.

Warren AC, Petersen MB, Van Hul W, McInnis MG, Van Broeckhoven C, Cox TK, Chakravarti A, Antonarakis SE. Warren AC, et al. Among authors: van broeckhoven c, van hul w. Genomics. 1992 Aug;13(4):1365-7. doi: 10.1016/0888-7543(92)90072-z. Genomics. 1992. PMID: 1505976

4

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.

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

The pericentromeric 21 DNA marker pGSM21 (D21S13) contains an expressed HTF island.

Stinissen P, Van Hul W, Van Camp G, Backhovens H, Wehnert A, Vandenberghe A, Van Broeckhoven C. Stinissen P, et al. Among authors: van broeckhoven c, van hul w, van camp g. Genomics. 1990 May;7(1):119-22. doi: 10.1016/0888-7543(90)90527-2. Genomics. 1990. PMID: 1692297

7

Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch).

Van Broeckhoven C, Haan J, Bakker E, Hardy JA, Van Hul W, Wehnert A, Vegter-Van der Vlis M, Roos RA. Van Broeckhoven C, et al. Among authors: van hul w. Science. 1990 Jun 1;248(4959):1120-2. doi: 10.1126/science.1971458. Science. 1990. PMID: 1971458

8

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

9

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

10

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

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