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Showing results (161-170 of 185) with videos related to

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Blood|November 5, 1997
Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemiaP Peeters, S D Raynaud, J Cools, et al.
Leukemia|August 22, 2003
Translocations t(11;18)(q21;q21) and t(14;18)(q32;q21) are the main chromosomal abnormalities involving MLT/MALT1 in MALT lymphomasE M Murga Penas, K Hinz, K Röser, et al.
Journal of Medical Genetics|January 15, 2003
A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patientsI Longo, S G M Frints, J-P Fryns, et al.
Blood|May 26, 1999
The apoptosis inhibitor gene API2 and a novel 18q gene, MLT, are recurrently rearranged in the t(11;18)(q21;q21) associated with mucosa-associated lymphoid tissue lymphomasJ Dierlamm, M Baens, I Wlodarska, et al.
Genes, Chromosomes & Cancer|February 15, 2001
Molecular cytogenetic and clinical findings in ETV6/ABL1-positive leukemiaH Van Limbergen, H B Beverloo, E van Drunen, et al.
Leukemia|August 30, 2002
The novel t(11;12;18)(q21;q13;q21) represents a variant translocation of the t(11;18)(q21;q21) associated with MALT-type lymphomaJ Dierlamm, E M Murga Penas, M Daibata, et al.
Blood|July 15, 1996
Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromesS D Raynaud, M Baens, J Grosgeorge, et al.
Journal of Medical Genetics|September 3, 2004
Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype mapG Van Buggenhout, C Melotte, B Dutta, et al.
Clinical Genetics|October 30, 2009
Novel PORCN mutations in focal dermal hypoplasiaG Froyen, K Govaerts, H Van Esch, et al.
American Journal of Human Genetics|March 26, 1999
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1K Devriendt, G Matthijs, R Van Dael, et al.
Pageof 19

Showing results (161-170 of 185) with videos related to

Sort By:
Pageof 19
Blood|November 5, 1997
Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemiaP Peeters, S D Raynaud, J Cools, et al.
Leukemia|August 22, 2003
Translocations t(11;18)(q21;q21) and t(14;18)(q32;q21) are the main chromosomal abnormalities involving MLT/MALT1 in MALT lymphomasE M Murga Penas, K Hinz, K Röser, et al.
Journal of Medical Genetics|January 15, 2003
A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patientsI Longo, S G M Frints, J-P Fryns, et al.
Blood|May 26, 1999
The apoptosis inhibitor gene API2 and a novel 18q gene, MLT, are recurrently rearranged in the t(11;18)(q21;q21) associated with mucosa-associated lymphoid tissue lymphomasJ Dierlamm, M Baens, I Wlodarska, et al.
Genes, Chromosomes & Cancer|February 15, 2001
Molecular cytogenetic and clinical findings in ETV6/ABL1-positive leukemiaH Van Limbergen, H B Beverloo, E van Drunen, et al.
Leukemia|August 30, 2002
The novel t(11;12;18)(q21;q13;q21) represents a variant translocation of the t(11;18)(q21;q21) associated with MALT-type lymphomaJ Dierlamm, E M Murga Penas, M Daibata, et al.
Blood|July 15, 1996
Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromesS D Raynaud, M Baens, J Grosgeorge, et al.
Journal of Medical Genetics|September 3, 2004
Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype mapG Van Buggenhout, C Melotte, B Dutta, et al.
Clinical Genetics|October 30, 2009
Novel PORCN mutations in focal dermal hypoplasiaG Froyen, K Govaerts, H Van Esch, et al.
American Journal of Human Genetics|March 26, 1999
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1K Devriendt, G Matthijs, R Van Dael, et al.
Pageof 19