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Showing results (61-70 of 77) with videos related to

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Human Molecular Genetics|December 1, 1994
Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogeneL M Mulligan, C Eng, T Attié, et al.
Cancer Genetics and Cytogenetics|May 1, 1996
Dicentric (1;15) in myeloid disordersL Michaux, J Dierlamm, C Mecucci, et al.
Human Mutation|January 15, 1999
Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseasesJ Poncin, R Abs, B Velkeniers, et al.
Genomics|February 1, 1988
A deletion hot spot in the Duchenne muscular dystrophy geneM C Wapenaar, T Kievits, K A Hart, et al.
Brain : a Journal of Neurology|March 10, 1999
The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotypeP De Jonghe, V Timmerman, C Ceuterick, et al.
Neurology|May 27, 2006
A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36I Maystadt, M Zarhrate, D Leclair-Richard, et al.
Cell|March 2, 1992
Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenitaA I McClatchey, P Van den Bergh, M A Pericak-Vance, et al.
Annals of Hematology|June 28, 2000
The value of interphase fluorescence in situ hybridization for the detection of translocation t(12;21) in childhood acute lymphoblastic leukemiaG Ameye, C Jacquy, A Zenebergh, et al.
Journal of Medical Genetics|February 9, 1999
Familial adenomatous polyposis associated with multiple adrenal adenomas in a patient with a rare 3' APC mutationA Kartheuser, C Walon, S West, et al.
Genes, Chromosomes & Cancer|August 5, 2000
MLL amplification in myeloid leukemias: A study of 14 cases with multiple copies of 11q23L Michaux, I Wlodarska, M Stul, et al.
Pageof 8

Showing results (61-70 of 77) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|December 1, 1994
Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogeneL M Mulligan, C Eng, T Attié, et al.
Cancer Genetics and Cytogenetics|May 1, 1996
Dicentric (1;15) in myeloid disordersL Michaux, J Dierlamm, C Mecucci, et al.
Human Mutation|January 15, 1999
Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseasesJ Poncin, R Abs, B Velkeniers, et al.
Genomics|February 1, 1988
A deletion hot spot in the Duchenne muscular dystrophy geneM C Wapenaar, T Kievits, K A Hart, et al.
Brain : a Journal of Neurology|March 10, 1999
The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotypeP De Jonghe, V Timmerman, C Ceuterick, et al.
Neurology|May 27, 2006
A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36I Maystadt, M Zarhrate, D Leclair-Richard, et al.
Cell|March 2, 1992
Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenitaA I McClatchey, P Van den Bergh, M A Pericak-Vance, et al.
Annals of Hematology|June 28, 2000
The value of interphase fluorescence in situ hybridization for the detection of translocation t(12;21) in childhood acute lymphoblastic leukemiaG Ameye, C Jacquy, A Zenebergh, et al.
Journal of Medical Genetics|February 9, 1999
Familial adenomatous polyposis associated with multiple adrenal adenomas in a patient with a rare 3' APC mutationA Kartheuser, C Walon, S West, et al.
Genes, Chromosomes & Cancer|August 5, 2000
MLL amplification in myeloid leukemias: A study of 14 cases with multiple copies of 11q23L Michaux, I Wlodarska, M Stul, et al.
Pageof 8