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A D Paepe

Showing results (1-10 of 4) with videos related to

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The British Journal of Dermatology|May 22, 2001
Acrogeric phenotype in Ehlers-Danlos syndrome type IV attributed to a missense mutation in the COL3A1 geneT Jansen, A D Paepe, L Nuytinck, et al.
Nucleic Acids Research|July 4, 2001
Quantification of splice variants using real-time PCRI I Vandenbroucke, J Vandesompele, A D Paepe, et al.
Human Mutation|June 22, 2000
Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defectsL M Messiaen, T Callens, G Mortier, et al.
Leukemia|October 14, 2006
Clinical, cytogenetic and molecular characteristics of 14 T-ALL patients carrying the TCRbeta-HOXA rearrangement: a study of the Groupe Francophone de Cytogénétique HématologiqueB Cauwelier, H Cavé, C Gervais, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
The British Journal of Dermatology|May 22, 2001
Acrogeric phenotype in Ehlers-Danlos syndrome type IV attributed to a missense mutation in the COL3A1 geneT Jansen, A D Paepe, L Nuytinck, et al.
Nucleic Acids Research|July 4, 2001
Quantification of splice variants using real-time PCRI I Vandenbroucke, J Vandesompele, A D Paepe, et al.
Human Mutation|June 22, 2000
Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defectsL M Messiaen, T Callens, G Mortier, et al.
Leukemia|October 14, 2006
Clinical, cytogenetic and molecular characteristics of 14 T-ALL patients carrying the TCRbeta-HOXA rearrangement: a study of the Groupe Francophone de Cytogénétique HématologiqueB Cauwelier, H Cavé, C Gervais, et al.
Pageof 1