Del-Favero J - Search Results

1

YAC fragmentation with repetitive and single-copy sequences: detailed physical mapping of the presenilin 1 gene on chromosome 14.

Del-Favero J, Goossens D, Van den Bossche D, Van Broeckhoven C. Del-Favero J, et al. Gene. 1999 Mar 18;229(1-2):193-201. doi: 10.1016/s0378-1119(99)00023-2. Gene. 1999. PMID: 10095119

2

Determination of the genomic organization of human presenilin 1 by fiber-FISH analysis and restriction mapping of cloned DNA.

Theuns J, Cruts M, Del-Favero J, Goossens D, Dauwerse H, Wehnert A, den Dunnen JT, Van Broeckhoven C. Theuns J, et al. Mamm Genome. 1999 Apr;10(4):410-4. doi: 10.1007/s003359901013. Mamm Genome. 1999. PMID: 10087304 No abstract available.

3

Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder.

Verheyen GR, Villafuerte SM, Del-Favero J, Souery D, Mendlewicz J, Van Broeckhoven C, Raeymaekers P. Verheyen GR, et al. Eur J Hum Genet. 1999 May-Jun;7(4):427-34. doi: 10.1038/sj.ejhg.5200318. Eur J Hum Genet. 1999. PMID: 10352933

4

No evidence for the involvement of CAG/CTG repeats from within 18q21.33-q23 in bipolar disorder.

Goossens D, Villafuerte S, Tissir F, Van Gestel S, Claes S, Souery D, Massat I, Van den Bossche D, Van Zand K, Mendlewicz J, Van Broeckhoven C, Del-Favero J. Goossens D, et al. Eur J Hum Genet. 2000 May;8(5):385-8. doi: 10.1038/sj.ejhg.5200469. Eur J Hum Genet. 2000. PMID: 10854100

5

Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation.

Del-Favero J, Goossens D, De Jonghe P, Benson K, Michalik A, Van den Bossche D, Horwitz M, Van Broeckhoven C. Del-Favero J, et al. Hum Genet. 1999 Sep;105(3):217-25. doi: 10.1007/s004390051092. Hum Genet. 1999. PMID: 10987648

6

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. Hum Mol Genet. 1998 Feb;7(2):177-86. doi: 10.1093/hmg/7.2.177. Hum Mol Genet. 1998. PMID: 9425224

7

A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes.

Wang SY, Cruts M, Del-Favero J, Zhang Y, Tissir F, Potier MC, Patterson D, Nizetic D, Bosch A, Chen H, Bennett L, Estivill X, Kessling A, Antonarakis SE, van Broeckhoven C. Wang SY, et al. Genome Res. 1999 Nov;9(11):1059-73. doi: 10.1101/gr.9.11.1059. Genome Res. 1999. PMID: 10568746 Free PMC article.

8

Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration.

Michalík A, Del-Favero J, Mauger C, Löfgren A, Van Broeckhoven C. Michalík A, et al. Hum Genet. 1999 Nov;105(5):410-7. doi: 10.1007/s004390051123. Hum Genet. 1999. PMID: 10598805

9

Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression.

Theuns J, Del-Favero J, Dermaut B, van Duijn CM, Backhovens H, Van den Broeck MV, Serneels S, Corsmit E, Van Broeckhoven CV, Cruts M. Theuns J, et al. Hum Mol Genet. 2000 Feb 12;9(3):325-31. doi: 10.1093/hmg/9.3.325. Hum Mol Genet. 2000. PMID: 10655540 Free article.

10

The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease.

Theuns J, Feuk L, Dermaut B, Del-Favero J, Roks G, Van den Bossche D, Corsmit E, Van den Broeck M, van Duijn CM, Cruts M, Brookes AJ, Van Broeckhoven C. Theuns J, et al. Hum Genet. 2001 Jun;108(6):552-3. doi: 10.1007/s004390100508. Hum Genet. 2001. PMID: 11499683 No abstract available.

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