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X monosomy and balanced Robertsonian translocation in a girl with Turner Syndrome
(Sociedade Brasileira de Genética, 2006-01-01)
We describe a case of X monosomy associated with a maternally inherited t(13;14) Robertsonian translocation in a girl with Turner syndrome. The girl's X chromosome was demonstrated to be maternally inherited, ruling out ...
Clonal monosomy of chromosome 21 in a case of myelodysplastic syndrome
(Funpec-editora, 2011-01-01)
This study reports on a cytogenetic finding in a bone marrow examination of a 47-year-old male patient treated in the Hematology and Blood Transfusion Service of the Hospital de Base in Sao Jose do Rio Preto, Sao Paulo ...
X monosomy and balanced Robertsonian translocation in a girl with Turner Syndrome
(Sociedade Brasileira de Genética, 2006-01-01)
We describe a case of X monosomy associated with a maternally inherited t(13;14) Robertsonian translocation in a girl with Turner syndrome. The girl's X chromosome was demonstrated to be maternally inherited, ruling out ...
Clonal monosomy of chromosome 21 in a case of myelodysplastic syndrome
(Funpec-editora, 2015)
X monosomy and balanced Robertsonian translocation in a girl with Turner Syndrome
(Sociedade Brasileira de Genética, 2014)
Clonal monosomy of chromosome 21 in a case of myelodysplastic syndrome
(Funpec-editora, 2015)
B lineage acute lymphoblastic leukemia transformation in a child with juvenile myelomonocytic leukemia, type 1 neurofibromatosis and monosomy of chromosome 7 - Possible implications in the leukemogenesis
(Elsevier B.V., 2003-04-01)
This report describes the case of an 8-month-old infant with a diagnosis of juvenile myelomonocytic leukemia (JMML) and type I neurofibromatosis that presented progression to B lineage acute lymphoid leukemia (ALL). The ...
B lineage acute lymphoblastic leukemia transformation in a child with juvenile myelomonocytic leukemia, type 1 neurofibromatosis and monosomy of chromosome 7 - Possible implications in the leukemogenesis
(Elsevier B.V., 2003-04-01)
This report describes the case of an 8-month-old infant with a diagnosis of juvenile myelomonocytic leukemia (JMML) and type I neurofibromatosis that presented progression to B lineage acute lymphoid leukemia (ALL). The ...