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European Journal of Haematology
|
June 11, 2015
Gender and BCR-ABL transcript type are correlated with molecular response to imatinib treatment in patients with chronic myeloid leukemia
Han-Xin Lin, Jenny Sjaarda, Jocob Dyck, et al.
European Journal of Haematology
|
October 19, 2016
Clinical evaluation of a hemochromatosis next-generation sequencing gene panel
Matthew B Lanktree, Bekim Sadikovic, John S Waye, et al.
Plos One
|
March 14, 2009
Discovery of novel hypermethylated genes in prostate cancer using genomic CpG island microarrays
Ken Kron, Vaijayanti Pethe, Laurent Briollais, et al.
American Journal of Medical Genetics. Part A
|
January 18, 2022
Near complete deletion of KMT2D in a college student
Catherine Gooch, Jaclyn Paige Souder, Matthew L Tedder, et al.
European Journal of Medical Genetics
|
July 5, 2022
Contribution of DNA methylation profiling to the reclassification of a variant of uncertain significance in the KDM5C gene
Juliette Coursimault, Alice Goldenberg, Gaël Nicolas, et al.
American Journal of Hematology
|
January 19, 2022
Serum erythropoietin levels in 696 patients investigated for erythrocytosis with JAK2 mutation analysis
Benjamin Chin-Yee, Ian Cheong, Maxim Matyashin, et al.
Plos One
|
December 29, 2010
Sequence homology at the breakpoint and clinical phenotype of mitochondrial DNA deletion syndromes
Bekim Sadikovic, Jing Wang, Ayman W El-Hattab, et al.
Plos One
|
November 21, 2017
Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
Bekim Sadikovic, Jing Wang, Ayman W El-Hattab, et al.
Human Genetics
|
July 19, 2024
The missing link: ARID1B non-truncating variants causing Coffin-Siris syndrome due to protein aggregation
Elisabeth Bosch, Esther Güse, Philipp Kirchner, et al.
American Journal of Medical Genetics. Part A
|
March 19, 2025
Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2 -Related Disorders to a Syndromic Multiple Tumor Phenotype
Marie Lucain, Antonio Vitobello, Bekim Sadikovic, et al.
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of 23
Search research articles
Search
Showing results (71-80 of 228) with videos related to
Sort By:
Page
of 23
European Journal of Haematology
|
June 11, 2015
Gender and BCR-ABL transcript type are correlated with molecular response to imatinib treatment in patients with chronic myeloid leukemia
Han-Xin Lin, Jenny Sjaarda, Jocob Dyck, et al.
European Journal of Haematology
|
October 19, 2016
Clinical evaluation of a hemochromatosis next-generation sequencing gene panel
Matthew B Lanktree, Bekim Sadikovic, John S Waye, et al.
Plos One
|
March 14, 2009
Discovery of novel hypermethylated genes in prostate cancer using genomic CpG island microarrays
Ken Kron, Vaijayanti Pethe, Laurent Briollais, et al.
American Journal of Medical Genetics. Part A
|
January 18, 2022
Near complete deletion of KMT2D in a college student
Catherine Gooch, Jaclyn Paige Souder, Matthew L Tedder, et al.
European Journal of Medical Genetics
|
July 5, 2022
Contribution of DNA methylation profiling to the reclassification of a variant of uncertain significance in the KDM5C gene
Juliette Coursimault, Alice Goldenberg, Gaël Nicolas, et al.
American Journal of Hematology
|
January 19, 2022
Serum erythropoietin levels in 696 patients investigated for erythrocytosis with JAK2 mutation analysis
Benjamin Chin-Yee, Ian Cheong, Maxim Matyashin, et al.
Plos One
|
December 29, 2010
Sequence homology at the breakpoint and clinical phenotype of mitochondrial DNA deletion syndromes
Bekim Sadikovic, Jing Wang, Ayman W El-Hattab, et al.
Plos One
|
November 21, 2017
Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
Bekim Sadikovic, Jing Wang, Ayman W El-Hattab, et al.
Human Genetics
|
July 19, 2024
The missing link: ARID1B non-truncating variants causing Coffin-Siris syndrome due to protein aggregation
Elisabeth Bosch, Esther Güse, Philipp Kirchner, et al.
American Journal of Medical Genetics. Part A
|
March 19, 2025
Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2 -Related Disorders to a Syndromic Multiple Tumor Phenotype
Marie Lucain, Antonio Vitobello, Bekim Sadikovic, et al.
Page
of 23