Wehnert A - Search Results

1

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: wehnert a. Hum Genet. 1989 Feb;81(3):231-3. doi: 10.1007/BF00278994. Hum Genet. 1989. PMID: 2921030

2

Dinucleotide repeat polymorphism at the D21S258 locus.

Wehnert A, Cruts M, Backhovens H, Delabar JM, Thomas G, Van Broeckhoven C. Wehnert A, et al. Hum Mol Genet. 1992 Sep;1(6):449. doi: 10.1093/hmg/1.6.449. Hum Mol Genet. 1992. PMID: 1339475 No abstract available.

3

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: wehnert a. Hum Genet. 1991 Oct;87(6):649-53. doi: 10.1007/BF00201718. Hum Genet. 1991. PMID: 1682232

4

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

5

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: wehnert a. Hum Genet. 1991 Jun;87(2):109-11. doi: 10.1007/BF00204162. Hum Genet. 1991. PMID: 2066096

6

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: wehnert a. Hum Genet. 1989 Aug;83(1):58-60. doi: 10.1007/BF00274149. Hum Genet. 1989. PMID: 2570018

7

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

8

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: wehnert a. Hum Genet. 1988 Jan;78(1):76-8. doi: 10.1007/BF00291239. Hum Genet. 1988. PMID: 2892777

9

Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.

Del-Favero J, Krols L, Michalik A, Theuns J, Löfgren A, Goossens D, Wehnert A, Van den Bossche D, Van Zand K, Backhovens H, van Regenmorter N, Martin JJ, Van Broeckhoven C. Del-Favero J, et al. Among authors: wehnert a. Hum Mol Genet. 1998 Feb;7(2):177-86. doi: 10.1093/hmg/7.2.177. Hum Mol Genet. 1998. PMID: 9425224

10

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: wehnert a. Genomics. 1990 May;7(1):119-22. doi: 10.1016/0888-7543(90)90527-2. Genomics. 1990. PMID: 1692297

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