Recommandations pour la prise en charge cytogélnétique des syndromes myéloprolifératifs autres que la leucémie myélöde chronique (LMC) établies par le Groupe Français de Cytogénétique Hématologique (GFCH)
GFCH doi: 10.1016/j.patbio.2004.04.003
GFCH (2004) Recommandations pour la prise en charge cytogélnétique des syndromes myéloprolifératifs autres que la leucémie myélöde chronique (LMC) établies par le Groupe Français de Cytogénétique Hématologique (GFCH). Pathol Biol 52:241-244. doi: 10.1016/j.patbio.2004.04.003
Clinical and molecular cytogenetic studies in seven patients with myeloid diseases characterized by i(20q-)
doi: 10.1111/j.1365-2141.2004.04921.x
Li T, Xue Y, Wu Y, Pan J (2004) Clinical and molecular cytogenetic studies in seven patients with myeloid diseases characterized by i(20q-). Br J Haematol 125:337-342. doi: 10.1111/j.1365-2141.2004.04921.x
Isochromosome of a deleted 20q: A rare but recurrent chromosome abnormality in myelodysplastic syndromes
doi: 10.1016/j.cancergencyto.2004.03.018
Saunders K, Czepulkowski B, Sivalingam R, Hayes JPLA, Aldouri M, Sekhar M, Cummins M, Ho A, Mufti GJ (2005) Isochromosome of a deleted 20q: A rare but recurrent chromosome abnormality in myelodysplastic syndromes. Cancer Genet Cytogenet 156:154-157. doi: 10.1016/ j.cancergencyto.2004.03.018
A novel isoderivative chromosome 20 in a patient with chronic myelomonocytic leukemia
doi: 10.1016/j.cancergencyto.2006.04.005
Lim TH, Lim AS, Tien SL (2006) A novel isoderivative chromosome 20 in a patient with chronic myelomonocytic leukemia. Cancer Genet Cytogenet 170:80-82. doi: 10.1016/j.cancergencyto.2006.04.005
Isoderivative chromosome 20 in bone marrow: Three new cases
doi: 10.1016/j.cancergencyto.2008.03.003
Shetty S, Roland B (2008) Isoderivative chromosome 20 in bone marrow: three new cases. Cancer Genet Cytogenet 184:72-73. doi: 10.1016/ j.cancergencyto.2008.03.003
Fluorescence in situ hybridization characterization of ider(20q) in myelodysplastic syndrome
doi: 10.1111/j.1365-2141.2008.07436.x
Douet-Guilbert N, Lai JL, Basinko A, Gueganic N, Andrieux J, Pollet B, Plantier I, Delattre C, Crepin O, Corm S, Le Bris MJ, Morel F, De Braekeleer M (2008) Fluorescence in situ hybridization characterization of ider(20q) in myelodysplastic syndrome. Br J Haematol 143:716-720. doi: 10.1111/j.1365-2141.2008.07436.x
Cytogenetic abnormalities and prognostic significance in idiopathic myelofibrosis: A study of 106 cases
doi: 10.1046/j.1365-2141.1997.1722990.x
Reilly JT, Snowden JA, Spearing RL, Fitzgerald PM, Jones N, Watmore A, Potter A (1997) Cytogenetic abnormalities and prognostic significance in idiopathic myelofibrosis: A study of 106 cases. Br J Haematol 98:96-102. doi: 10.1046/j.1365-2141.1997.1722990.x
Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: Characterization by molecular cytogenetics of commonly deleted and retained regions
doi: 10.1007/s00277-008-0462-3
Douet-Guilbert N, Basinko A, Morel F, Le Bris MJ, Ugo V, Morice P, Berthou C, De Braekeleer M (2008) Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: Characterization by molecular cytogenetics of commonly deleted and retained regions. Ann Hematol 87:537-544. doi: 10.1007/s00277-008-0462-3