Van Broeckhoven C - Search Results

1

Unique sequence homology in the pericentromeric regions of the long arms of chromosomes 13 and 21.

Van Camp G, Cruts M, Backhovens H, Wehnert A, Van Broeckhoven C. Van Camp G, et al. Among authors: van broeckhoven c. Genomics. 1992 Jan;12(1):158-60. doi: 10.1016/0888-7543(92)90420-w. Genomics. 1992. PMID: 1733854

2

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

3

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

4

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

5

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

6

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

7

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

8

Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphisms.

Stinissen P, Van Roy B, Van Camp G, Backhovens H, Partoens P, Wehnert A, Verniers H, Dumon J, Vandenberghe A, Van Broeckhoven C. Stinissen P, et al. Among authors: van roy b, van broeckhoven c, van camp g. Am J Med Genet Suppl. 1990;7:133-6. doi: 10.1002/ajmg.1320370727. Am J Med Genet Suppl. 1990. PMID: 1981473

9

A polymorphic locus [D21S144] is detected by probe pVC12 on chromosome 21.

Van Camp G, Stinissen P, Vandenberghe A, Van Broeckhoven C. Van Camp G, et al. Among authors: van broeckhoven c. Nucleic Acids Res. 1989 Jun 12;17(11):4420. doi: 10.1093/nar/17.11.4420. Nucleic Acids Res. 1989. PMID: 2567984 Free PMC article.

10

Absence of genetic linkage of Charcot-Marie-Tooth disease (HMSN Ia) with chromosome 1 gene markers.

Raeymaekers P, De Jonghe P, Backhovens H, Wehnert A, De Winter G, Swerts L, Gheuens J, Martin JJ, Vandenberghe A, Van Broeckhoven C. Raeymaekers P, et al. Among authors: van broeckhoven c. Neurology. 1989 Jun;39(6):844-6. doi: 10.1212/wnl.39.6.844. Neurology. 1989. PMID: 2725880

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