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Plos One
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May 16, 2013
Generation and characterization of an Nxf7 knockout mouse to study NXF5 deficiency in a patient with intellectual disability
Lieselot Vanmarsenille, Jelle Verbeeck, Stefanie Belet, et al.
Human Molecular Genetics
|
May 13, 2005
Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis
Hilde Van Esch, Karen Hollanders, Liesbeth Badisco, et al.
Gastroenterology
|
November 8, 2006
Intestinal neurofibromatosis is a subtype of familial GIST and results from a dominant activating mutation in PDGFRA
Thomas de Raedt, Jan Cools, Maria Debiec-Rychter, et al.
Cancer Genetics and Cytogenetics
|
June 19, 2007
Molecular cytogenetic findings in a four-way t(1;12;5;12)(p36;p13;q33;q24) underlying the ETV6-PDGFRB fusion gene in chronic myelomonocytic leukemia
Barbara Crescenzi, Roberta La Starza, Chiara Nozzoli, et al.
Haematologica
|
March 17, 2004
Submicroscopic deletions in 5q- associated malignancies
Barbara Crescenzi, Roberta La Starza, Silvia Romoli, et al.
Haematologica
|
October 3, 2009
T-cell/histiocyte-rich large B-cell lymphoma shows transcriptional features suggestive of a tolerogenic host immune response
Peter Van Loo, Thomas Tousseyn, Vera Vanhentenrijk, et al.
American Journal of Medical Genetics. Part A
|
April 17, 2014
Evidence for increased SOX3 dosage as a risk factor for X-linked hypopituitarism and neural tube defects
Marijke Bauters, Suzanna G Frints, Hilde Van Esch, et al.
Gastroenterology
|
February 3, 2005
Mechanisms of resistance to imatinib mesylate in gastrointestinal stromal tumors and activity of the PKC412 inhibitor against imatinib-resistant mutants
Maria Debiec-Rychter, Jan Cools, Herlinde Dumez, et al.
Nature Biotechnology
|
May 9, 2006
Gene prioritization through genomic data fusion
Stein Aerts, Diether Lambrechts, Sunit Maity, et al.
Blood
|
February 18, 2011
JAK2 rearrangements, including the novel SEC31A-JAK2 fusion, are recurrent in classical Hodgkin lymphoma
Katrien Van Roosbroeck, Luk Cox, Thomas Tousseyn, et al.
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of 10
Search research articles
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Showing results (51-60 of 92) with videos related to
Sort By:
Page
of 10
Plos One
|
May 16, 2013
Generation and characterization of an Nxf7 knockout mouse to study NXF5 deficiency in a patient with intellectual disability
Lieselot Vanmarsenille, Jelle Verbeeck, Stefanie Belet, et al.
Human Molecular Genetics
|
May 13, 2005
Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis
Hilde Van Esch, Karen Hollanders, Liesbeth Badisco, et al.
Gastroenterology
|
November 8, 2006
Intestinal neurofibromatosis is a subtype of familial GIST and results from a dominant activating mutation in PDGFRA
Thomas de Raedt, Jan Cools, Maria Debiec-Rychter, et al.
Cancer Genetics and Cytogenetics
|
June 19, 2007
Molecular cytogenetic findings in a four-way t(1;12;5;12)(p36;p13;q33;q24) underlying the ETV6-PDGFRB fusion gene in chronic myelomonocytic leukemia
Barbara Crescenzi, Roberta La Starza, Chiara Nozzoli, et al.
Haematologica
|
March 17, 2004
Submicroscopic deletions in 5q- associated malignancies
Barbara Crescenzi, Roberta La Starza, Silvia Romoli, et al.
Haematologica
|
October 3, 2009
T-cell/histiocyte-rich large B-cell lymphoma shows transcriptional features suggestive of a tolerogenic host immune response
Peter Van Loo, Thomas Tousseyn, Vera Vanhentenrijk, et al.
American Journal of Medical Genetics. Part A
|
April 17, 2014
Evidence for increased SOX3 dosage as a risk factor for X-linked hypopituitarism and neural tube defects
Marijke Bauters, Suzanna G Frints, Hilde Van Esch, et al.
Gastroenterology
|
February 3, 2005
Mechanisms of resistance to imatinib mesylate in gastrointestinal stromal tumors and activity of the PKC412 inhibitor against imatinib-resistant mutants
Maria Debiec-Rychter, Jan Cools, Herlinde Dumez, et al.
Nature Biotechnology
|
May 9, 2006
Gene prioritization through genomic data fusion
Stein Aerts, Diether Lambrechts, Sunit Maity, et al.
Blood
|
February 18, 2011
JAK2 rearrangements, including the novel SEC31A-JAK2 fusion, are recurrent in classical Hodgkin lymphoma
Katrien Van Roosbroeck, Luk Cox, Thomas Tousseyn, et al.
Page
of 10