Van Hul W - Search Results

1

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

2

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

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

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

7

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

8

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

9

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

10

Germline mosaicism and Duchenne muscular dystrophy mutations.

Bakker E, Van Broeckhoven C, Bonten EJ, van de Vooren MJ, Veenema H, Van Hul W, Van Ommen GJ, Vandenberghe A, Pearson PL. Bakker E, et al. Among authors: van de vooren mj, van ommen gj, van broeckhoven c, van hul w. Nature. 1987 Oct 8-14;329(6139):554-6. doi: 10.1038/329554a0. Nature. 1987. PMID: 2889144

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