Familial Myeloproliferative Disorders

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dc.contributor.author Bellanné-Chantelot, Christine -
dc.contributor.author Plo, Isabelle -
dc.date.accessioned 2018-03-13T11:38:56Z
dc.date.available 2018-03-13T11:38:56Z
dc.date.issued 2016 -
dc.identifier.citation Christine, Bellanné-Chantelot ; Isabelle, Plo. Familial Myeloproliferative Disorders. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2016, 9, p. 502-505 -
dc.identifier.issn 1768-3262 -
dc.identifier.uri http://hdl.handle.net/2042/66077
dc.description.abstract Review on Familial Myeloproliferative Disorders, with data on clinics, and the genes involved. en
dc.language.iso en -
dc.publisher ARMGHM - Atlas Génétique des Cancers -
dc.relation Atlas of Genetics and Cytogenetics in Oncology and Haematology ; http://AtlasGeneticsOncology.org/Kprones/FamMyeloproliferID10180.html -
dc.relation.ispartofseries Atlas of Genetics and Cytogenetics in Oncology and Haematology en
dc.rights Open access resource - terms and conditions : http://irevues.inist.fr/utilisation -
dc.subject Familial en
dc.subject Myeloproliferative disorders en
dc.subject Hereditary erythrocytosis en
dc.subject Hereditary thrombocytosis en
dc.subject TERT en
dc.subject GSKIP en
dc.subject ATG2B en
dc.subject RBBP6 en
dc.subject.classification Kprones Section en
dc.subject.mesh Adolescent en
dc.subject.mesh Adult en
dc.subject.mesh Aged en
dc.subject.mesh Autophagy-Related Proteins en
dc.subject.mesh Child en
dc.subject.mesh Chromosomes, Human, Pair 14 en
dc.subject.mesh Female en
dc.subject.mesh *Gene Duplication en
dc.subject.mesh *Genetic Predisposition to Disease en
dc.subject.mesh *Germ Cells en
dc.subject.mesh Humans en
dc.subject.mesh Induced Pluripotent Stem Cells/cytology en
dc.subject.mesh Infant en
dc.subject.mesh Leukemia, Myeloid, Acute/*genetics en
dc.subject.mesh Male en
dc.subject.mesh Myelodysplastic Syndromes/*genetics en
dc.subject.mesh Pedigree en
dc.subject.mesh Phenotype en
dc.subject.mesh Repressor Proteins/*genetics en
dc.subject.mesh Vesicular Transport Proteins/*genetics en
dc.subject.mesh Young Adult en
dc.title Familial Myeloproliferative Disorders en
dc.type Article -
dc.contributor.affiliation Département de Génétique, Hôpitaux Universitaires Pitié-Salpétrière-Charles Foix, Paris (CBC) -
dc.contributor.affiliation INSERM UMR1170, Institut Gustave Roussy, Villejuif (CBC, IP), France -
dc.identifier.doi https://doi.org/10.4267/2042/66077


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