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Showing results (41-50 of 66) with videos related to

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American Journal of Medical Genetics. Part A|July 17, 2008
Array-CGH in a series of 30 patients with mental retardation, dysmorphic features, and congenital malformations detected an interstitial 1p22.2-p31.1 deletion in a patient with features overlapping the Goldenhar syndromeP Callier, L Faivre, C Thauvin-Robinet, et al.
American Journal of Medical Genetics. Part A|February 13, 2009
Polymicrogyria in a child with inv dup del(9p) and 22q11.2 microduplicationA L Mosca, P Callier, L Faivre, et al.
European Journal of Medical Genetics|August 28, 2007
Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24)P Callier, L Faivre, N Marle, et al.
JIMD Reports|January 29, 2015
Homozygous Truncating Intragenic Duplication in TUSC3 Responsible for Rare Autosomal Recessive Nonsyndromic Intellectual Disability with No Clinical or Biochemical Metabolic MarkersS El Chehadeh, C Bonnet, P Callier, 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.
The American Journal of Surgical Pathology|February 16, 1999
CD4+ CD56+ cutaneous neoplasms: a distinct hematological entity? Groupe Français d'Etude des Lymphomes Cutanés (GFELC)T Petrella, S Dalac, M Maynadié, et al.
Cancer Genetics and Cytogenetics|December 13, 2005
Cytogenetic study of 75 erythroleukemiasM Lessard, S Struski, V Leymarie, et al.
Cancer Genetics and Cytogenetics|June 19, 2007
Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome-acute myeloid leukemia actually differ?M Lessard, C Hélias, S Struski, et al.
Clinical Genetics|July 5, 2011
What can we learn from old microdeletion syndromes using array-CGH screening?A L Mosca-Boidron, S Bouquillon, L Faivre, et al.
Leukemia|June 6, 2008
Acute myeloid leukaemia with 8p11 (MYST3) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogénétique hématologiqueC Gervais, A Murati, C Helias, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics. Part A|July 17, 2008
Array-CGH in a series of 30 patients with mental retardation, dysmorphic features, and congenital malformations detected an interstitial 1p22.2-p31.1 deletion in a patient with features overlapping the Goldenhar syndromeP Callier, L Faivre, C Thauvin-Robinet, et al.
American Journal of Medical Genetics. Part A|February 13, 2009
Polymicrogyria in a child with inv dup del(9p) and 22q11.2 microduplicationA L Mosca, P Callier, L Faivre, et al.
European Journal of Medical Genetics|August 28, 2007
Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24)P Callier, L Faivre, N Marle, et al.
JIMD Reports|January 29, 2015
Homozygous Truncating Intragenic Duplication in TUSC3 Responsible for Rare Autosomal Recessive Nonsyndromic Intellectual Disability with No Clinical or Biochemical Metabolic MarkersS El Chehadeh, C Bonnet, P Callier, 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.
The American Journal of Surgical Pathology|February 16, 1999
CD4+ CD56+ cutaneous neoplasms: a distinct hematological entity? Groupe Français d'Etude des Lymphomes Cutanés (GFELC)T Petrella, S Dalac, M Maynadié, et al.
Cancer Genetics and Cytogenetics|December 13, 2005
Cytogenetic study of 75 erythroleukemiasM Lessard, S Struski, V Leymarie, et al.
Cancer Genetics and Cytogenetics|June 19, 2007
Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome-acute myeloid leukemia actually differ?M Lessard, C Hélias, S Struski, et al.
Clinical Genetics|July 5, 2011
What can we learn from old microdeletion syndromes using array-CGH screening?A L Mosca-Boidron, S Bouquillon, L Faivre, et al.
Leukemia|June 6, 2008
Acute myeloid leukaemia with 8p11 (MYST3) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogénétique hématologiqueC Gervais, A Murati, C Helias, et al.
Pageof 7