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Molecular Genetics & Genomic Medicine
|
July 29, 2016
The limitations of qPCR telomere length measurement in diagnosing dyskeratosis congenita
Shahinaz M Gadalla, Payal P Khincha, Hormuzd A Katki, et al.
Molecular Genetics & Genomic Medicine
|
May 7, 2021
The causes of Fanconi anemia in South Asia and the Middle East: A case series and review of the literature
Ashley S Thompson, Nusrat Saba, Lisa J McReynolds, et al.
Respiratory Medicine
|
June 17, 2019
Combined effects of lung function, blood gases and kidney function on the exacerbation risk in stable COPD: Results from the COSYCONET cohort
F C Trudzinski, K Kahnert, C F Vogelmeier, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
|
October 15, 2016
The Second Pediatric Blood and Marrow Transplant Consortium International Consensus Conference on Late Effects after Pediatric Hematopoietic Cell Transplantation: Defining the Unique Late Effects of Children Undergoing Hematopoietic Cell Transplantation for Immune Deficiencies, Inherited Marrow Failure Disorders, and Hemoglobinopathies
Andrew C Dietz, Christine N Duncan, Blanche P Alter, et al.
Human Molecular Genetics
|
February 7, 2001
Comparative genome analysis delimits a chromosomal domain and identifies key regulatory elements in the alpha globin cluster
J Flint, C Tufarelli, J Peden, et al.
British Journal of Haematology
|
May 12, 2010
Stable long-term risk of leukaemia in patients with severe congenital neutropenia maintained on G-CSF therapy
Philip S Rosenberg, Cornelia Zeidler, Audrey A Bolyard, et al.
Plos One
|
June 4, 2014
Dubowitz syndrome is a complex comprised of multiple, genetically distinct and phenotypically overlapping disorders
Douglas R Stewart, Alexander Pemov, Jennifer J Johnston, et al.
Blood
|
February 25, 2006
The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy
Philip S Rosenberg, Blanche P Alter, Audrey A Bolyard, et al.
British Journal of Haematology
|
November 22, 2007
Neutrophil elastase mutations and risk of leukaemia in severe congenital neutropenia
Philip S Rosenberg, Blanche P Alter, Daniel C Link, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
|
January 27, 2020
Population Frequency of Fanconi Pathway Gene Variants and Their Association with Survival After Hematopoietic Cell Transplantation for Severe Aplastic Anemia
Lisa J McReynolds, Youjin Wang, Ashley S Thompson, et al.
Page
of 37
Search research articles
Search
Showing results (311-320 of 362) with videos related to
Sort By:
Page
of 37
Molecular Genetics & Genomic Medicine
|
July 29, 2016
The limitations of qPCR telomere length measurement in diagnosing dyskeratosis congenita
Shahinaz M Gadalla, Payal P Khincha, Hormuzd A Katki, et al.
Molecular Genetics & Genomic Medicine
|
May 7, 2021
The causes of Fanconi anemia in South Asia and the Middle East: A case series and review of the literature
Ashley S Thompson, Nusrat Saba, Lisa J McReynolds, et al.
Respiratory Medicine
|
June 17, 2019
Combined effects of lung function, blood gases and kidney function on the exacerbation risk in stable COPD: Results from the COSYCONET cohort
F C Trudzinski, K Kahnert, C F Vogelmeier, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
|
October 15, 2016
The Second Pediatric Blood and Marrow Transplant Consortium International Consensus Conference on Late Effects after Pediatric Hematopoietic Cell Transplantation: Defining the Unique Late Effects of Children Undergoing Hematopoietic Cell Transplantation for Immune Deficiencies, Inherited Marrow Failure Disorders, and Hemoglobinopathies
Andrew C Dietz, Christine N Duncan, Blanche P Alter, et al.
Human Molecular Genetics
|
February 7, 2001
Comparative genome analysis delimits a chromosomal domain and identifies key regulatory elements in the alpha globin cluster
J Flint, C Tufarelli, J Peden, et al.
British Journal of Haematology
|
May 12, 2010
Stable long-term risk of leukaemia in patients with severe congenital neutropenia maintained on G-CSF therapy
Philip S Rosenberg, Cornelia Zeidler, Audrey A Bolyard, et al.
Plos One
|
June 4, 2014
Dubowitz syndrome is a complex comprised of multiple, genetically distinct and phenotypically overlapping disorders
Douglas R Stewart, Alexander Pemov, Jennifer J Johnston, et al.
Blood
|
February 25, 2006
The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy
Philip S Rosenberg, Blanche P Alter, Audrey A Bolyard, et al.
British Journal of Haematology
|
November 22, 2007
Neutrophil elastase mutations and risk of leukaemia in severe congenital neutropenia
Philip S Rosenberg, Blanche P Alter, Daniel C Link, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
|
January 27, 2020
Population Frequency of Fanconi Pathway Gene Variants and Their Association with Survival After Hematopoietic Cell Transplantation for Severe Aplastic Anemia
Lisa J McReynolds, Youjin Wang, Ashley S Thompson, et al.
Page
of 37