Isochromosome of the long arm of chromosome 7 is a known chromosomal abnormality in hematological malignancies that may be found in patients with Shwachman-Diamond syndrome, hepatosplenic T-cell lymphoma and acute lymphoblastic leukemia. In myeloid malignancies, i(7)(q10) may be found in acute myeloid leukemias and chronic myeloproliferative disorders, either as a solely anomaly or more frequently as a secondary anomaly associated with other additional anomalies
The World Health Organization classifies atypical chronic myeloid leukemia (aCML) as a myeloprolifer...
Review on i(17q) solely in myeloid malignancies, with data on clinics, and the genes involved
Shwachman syndrome (SS) is an autosomal recessive disorder in which bone marrow dysfunction is obser...
Isochromosome 7q, i(7)(q10), is a rare recurrent aberration found in various hematological neoplasms...
Isochromosome of the short arm of chromosome 5 is an infrequent chromosome anomaly that has been rep...
Isochromosome i(22)(q10) is a rare but non-random karyotypic change in hematologic malignancies, oft...
Complete or partial loss of chromosome 7 is a recurrent cytogenetic abnormality that may be observed...
Partial gain of the long arm of chromosome 11, containing the unrearranged mixed lineage leukaemia (...
Review on i(8)(q10) in acute myeloid leukaemia, with data on clinics, and the genes involved
Shwachman syndrome (SS) is an autosomal recessive disorder in which bone marrow dysfunction is obser...
Shwachman syndrome (SS) is an autosomal recessive disorder in which bone marrow dysfunction is obser...
Shwachman syndrome (SS) is an autosomal recessive disorder in which bone marrow dysfunction is obser...
Review on +7 or trisomy 7 (solely), with data on clinics, and the genes involved
The World Health Organization classifies atypical chronic myeloid leukemia (aCML) as a myeloprolifer...
The World Health Organization classifies atypical chronic myeloid leukemia (aCML) as a myeloprolifer...
The World Health Organization classifies atypical chronic myeloid leukemia (aCML) as a myeloprolifer...
Review on i(17q) solely in myeloid malignancies, with data on clinics, and the genes involved
Shwachman syndrome (SS) is an autosomal recessive disorder in which bone marrow dysfunction is obser...
Isochromosome 7q, i(7)(q10), is a rare recurrent aberration found in various hematological neoplasms...
Isochromosome of the short arm of chromosome 5 is an infrequent chromosome anomaly that has been rep...
Isochromosome i(22)(q10) is a rare but non-random karyotypic change in hematologic malignancies, oft...
Complete or partial loss of chromosome 7 is a recurrent cytogenetic abnormality that may be observed...
Partial gain of the long arm of chromosome 11, containing the unrearranged mixed lineage leukaemia (...
Review on i(8)(q10) in acute myeloid leukaemia, with data on clinics, and the genes involved
Shwachman syndrome (SS) is an autosomal recessive disorder in which bone marrow dysfunction is obser...
Shwachman syndrome (SS) is an autosomal recessive disorder in which bone marrow dysfunction is obser...
Shwachman syndrome (SS) is an autosomal recessive disorder in which bone marrow dysfunction is obser...
Review on +7 or trisomy 7 (solely), with data on clinics, and the genes involved
The World Health Organization classifies atypical chronic myeloid leukemia (aCML) as a myeloprolifer...
The World Health Organization classifies atypical chronic myeloid leukemia (aCML) as a myeloprolifer...
The World Health Organization classifies atypical chronic myeloid leukemia (aCML) as a myeloprolifer...
Review on i(17q) solely in myeloid malignancies, with data on clinics, and the genes involved
Shwachman syndrome (SS) is an autosomal recessive disorder in which bone marrow dysfunction is obser...