Vandenberghe A - Search Results

1

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: vandenberghe a. Somat Cell Mol Genet. 1990 May;16(3):241-9. doi: 10.1007/BF01233360. Somat Cell Mol Genet. 1990. PMID: 1972817

2

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: vandenberghe a. Am J Med Genet Suppl. 1990;7:133-6. doi: 10.1002/ajmg.1320370727. Am J Med Genet Suppl. 1990. PMID: 1981473

3

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: vandenberghe a. 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.

4

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: vandenberghe a. Neurology. 1989 Jun;39(6):844-6. doi: 10.1212/wnl.39.6.844. Neurology. 1989. PMID: 2725880

5

The Duffy blood group is linked to the alpha-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1.

Raeymaekers P, Van Broeckhoven C, Backhovens H, Wehnert A, Muylle L, De Jonghe P, Gheuens J, Vandenberghe A. Raeymaekers P, et al. Among authors: vandenberghe a. Hum Genet. 1988 Jan;78(1):76-8. doi: 10.1007/BF00291239. Hum Genet. 1988. PMID: 2892777

6

Linkage analysis of the Duffy blood group marker with several chromosome 1 genes in an extended pedigree with Charcot-Marie-Tooth disease.

Raeymaekers P, Van Broeckhoven C, Backhovens H, Wehnert A, Muylle L, De Jonghe P, Gheuens J, Martin JJ, Vandenberghe A. Raeymaekers P, et al. Among authors: vandenberghe a. Hum Genet. 1989 Feb;81(3):231-3. doi: 10.1007/BF00278994. Hum Genet. 1989. PMID: 2921030

7

A high frequency EcoRI RFLP detected at the D21S13 locus.

Stinissen P, Vandenberghe A, Van Broeckhoven C. Stinissen P, et al. Among authors: vandenberghe a. Nucleic Acids Res. 1990 Mar 11;18(5):1319. doi: 10.1093/nar/18.5.1319-a. Nucleic Acids Res. 1990. PMID: 1969629 Free PMC article.

8

PCR detection of two RFLP's at the D21S13 locus.

Stinissen P, Vandenberghe A, Van Broeckhoven C. Stinissen P, et al. Among authors: vandenberghe a. Nucleic Acids Res. 1990 Jun 25;18(12):3672. doi: 10.1093/nar/18.12.3672. Nucleic Acids Res. 1990. PMID: 1972981 Free PMC article.

9

Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12.

Timmerman V, Raeymaekers P, De Jonghe P, De Winter G, Swerts L, Jacobs K, Gheuens J, Martin JJ, Vandenberghe A, Van Broeckhoven C. Timmerman V, et al. Among authors: vandenberghe a. Am J Hum Genet. 1990 Oct;47(4):680-5. Am J Hum Genet. 1990. PMID: 2220808 Free PMC article.

10

[Genetic coupling study using DNA markers in the familial form of Alzheimer's disease].

Vandenberghe A, Van Broeckhoven C. Vandenberghe A, et al. Acta Neurol Belg. 1989 May-Oct;89(3-4):300-1. Acta Neurol Belg. 1989. PMID: 2516981 Dutch. No abstract available.

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