Atlas of Genetics and Cytogenetics in Oncology and Haematology


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Case Reports

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Case Reports

Table of Content

Dic(1;15)(p11;p11) as a non-random abnormality in Polycytemia Vera
Olivier Theisen, Steven Richebourg, Jean-Luc Lai, Catherine Roche-Lestienne
Dic(1;15)(p11;p11) as a non-random abnormality in Myelodysplasic syndrome
Olivier Theisen, Steven Richebourg, Jean-Luc Lai, Catherine Roche-Lestienne
Dic(1;15)(p11;p11) as a non-random abnormality in essential thrombocytemia
Olivier Theisen, Steven Richebourg, Jean-Luc Lai, Catherine Roche-Lestienne
Dic(1;15)(p11;p11) as a non-random abnormality in atypical MPD
Olivier Theisen, Steven Richebourg, Jean-Luc Lai, Catherine Roche-Lestienne
Translocation t(11;15)(q23;q14) detected in AML at first relapse
Elvira D Rodrigues Pereira Velloso, Silvia Helena Figueiredo, Cristina A Ratis, Ana Cláudia Brito, Nydia S Bacal, Yana AS Novis, Cristóvão LP Mangueira
A case of Chronic Lymphocytic Leukemia (CLL) with a rare chromosome abnormality: t(1;14;6)(q21;q32;p21), a variant of t(6;14)(p21;q32).
Alka Dwivedi, Thomas Casey, Siddharth G Adhvaryu
Translocation t(7;9)(q34;q32) found in pediatric T-cell Acute Lymphoblastic Leukemia
Jennifer JS Laffin, Randee J Blumer, Sara J Morrison-Delap, Elizabeth A Rauch, Eric B Johnson, Carol A Diamond, Kate J Thompson, Gordana Raca, Karen D Montgomery, Daniel F Kurtycz
A case of trisomy 8 and loss of the Y-chromosome as secondary aberrations in a ten year old boy with de novo AML FAB M2 and t(16;21)(q24;q22)
Jutta Bradtke, Peter Vorwerk, Jochen Harbott
Translocation t(1;6)(p35;p25) in B-cell lymphoproliferative disorder with evolution to Diffuse Large B-cell Lymphoma
Elvira D Rodrigues Pereira Velloso, Cristina Ratis, Sérgio A B Brasil, João Carlos Guerra, Nydia Bacal; Cristóvão P Mangueira LM Pitangueira
Translocation t(8;12)(q13;p13) in a case with acute leukemia of ambiguous lineage
Marta Gallego, Mariela Coccé, Andrea Bernasconi, Maria Felice, Cristina Alonso, Myriam Guitter
Translocation t(11;20)(p15;q11) detected in AML M0: A case report
Bani B Ganguly, Yogesh Loher, M B Agarwal
inv(8)(p11.2q13) found in a patient with chronic myelomonocytic leukemia that progressed to acute myeloid leukemia
Jennifer JS Laffin, Sara J Morrison-Delap, Wayne A Bottner, Eric B Johnson, Patricia Howard-Peebles, Kate J Thompson, Gordana Raca, Karen D Montgomery, Daniel F Kurtycz
t(3;4)(p21;q34) as a sole anomaly in acute myeloid leukemia patient
Adriana Zamecnikova
t(3;5)(q25;q35) as a sole anomaly in acute myeloid leukemia patient
Adriana Zamecnikova
t(1;16)(q11-12;q11) presented as a der(16)t(1;16) in a patient with acute lymphoblastic leukemia.
Adriana Zamecnikova
A t(4;12)(q11;p13) in a patient with coincident CLL at the same time of AML diagnosis
Paola Dal Cin, Daniel J DeAngelo, Richard M Stone
t(16;21)(q24;q22) in therapy-related acute myelogenous leukemia arising from myelodysplastic syndrome
Paola Dal Cin, Karim Ouahchi
A de novo AML with a t(1;21)(p36;q22) in an elderly patient
Paola Dal Cin, Andrew J Yee, Bimalangshu Dey
A novel chromosomal translocation (6;14) (p22;q32) in a case of precursor B-cell Acute Lymphoblastic Leukemia
Siddharth G Adhvaryu, Alka Dwivedi, Peggy Stoll
A case of myeloproliferative disorder with t(5;10)(q33;q21.2)
Valeria AS De Melo, Alistair G Reid
t(8;13)(p12;q12) in an atypical chronic myeloid leukaemia case
Valeria AS De Melo, Alistair G Reid
Reciprocal translocation t(2;12)(q31;p13) in a case of CMML
Despina Iakovaki, Markos Fisfis, Katy Stefanoudaki, Georgia Bardi
Isolated trisomy 2 is non-random and may be found in myelodysplastic syndrome and in acute myeloblastic leukaemia. Case 2
Catherine Roche-Lestienne, Agnès Charpentier, Sandrine Geffroy, Joris Andrieux, Jean-Loup Demory, Jean-Luc Laï
Isolated trisomy 2 is non-random and may be found in myelodysplastic syndrome and in acute myeloblastic leukaemia. Case 1
Catherine Roche-Lestienne, Agnès Charpentier, Sandrine Geffroy, Joris Andrieux, Jean-Loup Demory, Jean-Luc Laï
t(4;12)(q11;p13) in an acute myeloid leukemia without maturation with myelodysplasia
Jean Philippe Rault
A new case of t(16;21)(q24;q22) in a secondary AML-M2 following breast cancer therapy
Helene Bruyere, Wilson Yeung, Peter Tsang
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 4
Kavita S Reddy, Kathy Richkind
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 3
Kavita S Reddy, Kathy Richkind
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 2
Kavita S Reddy, Kathy Richkind
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 1
Kavita S. Reddy, Kathy Richkind
A new case of t(1;11)(q21;q23) in a child with M1 ANLL
Katell Le Du, Eric Jeandidier, Francine Garnache, Pierre Rohrlich, Jean-Luc Bresson, Marie-Agnès Collonge-Rame
A new case of t(8;14)(q11;q32) in an acute lymphoblastic leukemia
Benoit Quilichini, Helene Zattara, François Casalonga, Laure-Anne Bastide-Alliez, Catherine Curtillet, Chantal Fossat, Gérard Michel
Translocation t(2;19)(p11;p12-p13) in childhood with acute myeloid leukemia
Benoit Quilichini, Helene Zattara, Elodie Cas, Laure-Anne Bastide-Alliez, Annie Blachere, Catherine Curtillet, Chantal Fossat, Gérard Michel
The rare t(4;12)(q11;p13) in an elderly patient with de novo AML with multilineage dysplasia co-expressing stem cell markers
Sarah Moore, Sanjeev Chunilal, Jacqueline Beerworth
Pentasomy 21 as a sole abnormality in an atypical CML patient in chronic phase
Shambhu K Roy, Sonal R Bakshi, Shailesh J Patel, Pina J Trivedi, Manisha M Brahmbhatt, Shwetal M Rawal, Pankaj M Shah, Devendra D Patel
A case of Down syndrome with acute lymphoblastic leukemia and t(8;14)(q11;q32)
Petr Balicek, Jana Rabasova, Jiri Hak
A case of pre-B ALL with t(8;14)(q11;q32)
Gitte Birk Kerndrup, Steen Rosthøj

Study Groups

Nineteen Cases of the t(1;22)(p13;q13) Acute Megakaryoblastic Leukaemia of Infants/Children and a Review of 39 Cases : Report from a t(1;22) Study Group.
Jean-Loup Huret


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