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Showing results (241-250 of 362) with videos related to

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The American Journal of the Medical Sciences|August 1, 1997
Pure red cell aplasia associated with hepatitis C infectionY al-Awami, D A Sears, G Carrum, et al.
BMC Blood Disorders|June 17, 2011
Lung transplantation for pulmonary fibrosis in dyskeratosis congenita: Case Report and systematic literature reviewNeelam Giri, Rees Lee, Albert Faro, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
Complex phenotype of dyskeratosis congenita and mood dysregulation with novel homozygous RTEL1 and TPH1 variantsRachel A Ungar, Neelam Giri, Maryland Pao, et al.
Psychosomatics|March 31, 2012
Neuropsychiatric conditions among patients with dyskeratosis congenita: a link with telomere biology?Sandra Rackley, Maryland Pao, Guillermo F Seratti, et al.
British Journal of Haematology|May 30, 2013
Genetic regulation of fetal haemoglobin in inherited bone marrow failure syndromesBlanche P Alter, Philip S Rosenberg, Thomas Day, et al.
Blood|December 1, 2021
Disease progression and clinical outcomes in telomere biology disordersMarena R Niewisch, Neelam Giri, Lisa J McReynolds, et al.
Hemoglobin|January 1, 1992
Sickle and thalassemic erythroid progenitor cells are different from normalB P Alter, L He, R Acosta, et al.
Endocrine Connections|July 20, 2024
Reduced anti-Müllerian hormone levels in males with inherited bone marrow failure syndromesPamela Stratton, Neelam Giri, Sonia Bhala, et al.
Human Genetics|January 19, 2013
Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenitaBari J Ballew, Meredith Yeager, Kevin Jacobs, et al.
The New England Journal of Medicine|July 27, 1978
Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletionS H Orkin, B P Alter, C Altay, et al.
Pageof 37

Showing results (241-250 of 362) with videos related to

Sort By:
Pageof 37
The American Journal of the Medical Sciences|August 1, 1997
Pure red cell aplasia associated with hepatitis C infectionY al-Awami, D A Sears, G Carrum, et al.
BMC Blood Disorders|June 17, 2011
Lung transplantation for pulmonary fibrosis in dyskeratosis congenita: Case Report and systematic literature reviewNeelam Giri, Rees Lee, Albert Faro, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
Complex phenotype of dyskeratosis congenita and mood dysregulation with novel homozygous RTEL1 and TPH1 variantsRachel A Ungar, Neelam Giri, Maryland Pao, et al.
Psychosomatics|March 31, 2012
Neuropsychiatric conditions among patients with dyskeratosis congenita: a link with telomere biology?Sandra Rackley, Maryland Pao, Guillermo F Seratti, et al.
British Journal of Haematology|May 30, 2013
Genetic regulation of fetal haemoglobin in inherited bone marrow failure syndromesBlanche P Alter, Philip S Rosenberg, Thomas Day, et al.
Blood|December 1, 2021
Disease progression and clinical outcomes in telomere biology disordersMarena R Niewisch, Neelam Giri, Lisa J McReynolds, et al.
Hemoglobin|January 1, 1992
Sickle and thalassemic erythroid progenitor cells are different from normalB P Alter, L He, R Acosta, et al.
Endocrine Connections|July 20, 2024
Reduced anti-Müllerian hormone levels in males with inherited bone marrow failure syndromesPamela Stratton, Neelam Giri, Sonia Bhala, et al.
Human Genetics|January 19, 2013
Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenitaBari J Ballew, Meredith Yeager, Kevin Jacobs, et al.
The New England Journal of Medicine|July 27, 1978
Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletionS H Orkin, B P Alter, C Altay, et al.
Pageof 37