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Showing results (251-260 of 362) with videos related to

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The New England Journal of Medicine|May 11, 1978
Normal erythropoietic helper T cells in congenital hypoplastic (Diamond-Blackfan) anemiaD G Nathan, D G Hillman, L Chess, et al.
Retinal Cases & Brief Reports|November 13, 2014
Proliferative retinopathy as a complication of dyskeratosis congenitaJohn O Mason, Jacob J Yunker, Peter A Nixon, et al.
Pediatric Research|March 24, 2022
Shwachman Diamond syndrome: narrow genotypic spectrum and variable clinical featuresAshley S Thompson, Neelam Giri, D Matthew Gianferante, et al.
Blood|June 25, 1999
Embryonic hemoglobins are expressed in definitive cellsH Y Luo, X L Liang, C Frye, et al.
International Journal of Cancer|April 6, 2013
Squamous cell carcinomas in patients with Fanconi anemia and dyskeratosis congenita: a search for human papillomavirusBlanche P Alter, Neelam Giri, Sharon A Savage, et al.
American Journal of Medical Genetics. Part A|November 23, 2015
Novel FANCI mutations in Fanconi anemia with VACTERL associationSharon A Savage, Bari J Ballew, Neelam Giri, et al.
Acta Haematologica|January 1, 1997
A new syndrome of familial aplastic anemia and chronic liver diseaseM H Qazilbash, J M Liu, A Vlachos, et al.
Neurology. Genetics|December 25, 2019
CNS manifestations in patients with telomere biology disordersSonia Bhala, Ana F Best, Neelam Giri, et al.
British Journal of Haematology|December 21, 2012
Erythrocyte adenosine deaminase: diagnostic value for Diamond-Blackfan anaemiaJohn H Fargo, Christian P Kratz, Neelam Giri, et al.
Journal of the American Academy of Dermatology|October 19, 2017
Beyond the triad: Inheritance, mucocutaneous phenotype, and mortality in a cohort of patients with dyskeratosis congenitaSuzanne C Ward, Sharon A Savage, Neelam Giri, et al.
Pageof 37

Showing results (251-260 of 362) with videos related to

Sort By:
Pageof 37
The New England Journal of Medicine|May 11, 1978
Normal erythropoietic helper T cells in congenital hypoplastic (Diamond-Blackfan) anemiaD G Nathan, D G Hillman, L Chess, et al.
Retinal Cases & Brief Reports|November 13, 2014
Proliferative retinopathy as a complication of dyskeratosis congenitaJohn O Mason, Jacob J Yunker, Peter A Nixon, et al.
Pediatric Research|March 24, 2022
Shwachman Diamond syndrome: narrow genotypic spectrum and variable clinical featuresAshley S Thompson, Neelam Giri, D Matthew Gianferante, et al.
Blood|June 25, 1999
Embryonic hemoglobins are expressed in definitive cellsH Y Luo, X L Liang, C Frye, et al.
International Journal of Cancer|April 6, 2013
Squamous cell carcinomas in patients with Fanconi anemia and dyskeratosis congenita: a search for human papillomavirusBlanche P Alter, Neelam Giri, Sharon A Savage, et al.
American Journal of Medical Genetics. Part A|November 23, 2015
Novel FANCI mutations in Fanconi anemia with VACTERL associationSharon A Savage, Bari J Ballew, Neelam Giri, et al.
Acta Haematologica|January 1, 1997
A new syndrome of familial aplastic anemia and chronic liver diseaseM H Qazilbash, J M Liu, A Vlachos, et al.
Neurology. Genetics|December 25, 2019
CNS manifestations in patients with telomere biology disordersSonia Bhala, Ana F Best, Neelam Giri, et al.
British Journal of Haematology|December 21, 2012
Erythrocyte adenosine deaminase: diagnostic value for Diamond-Blackfan anaemiaJohn H Fargo, Christian P Kratz, Neelam Giri, et al.
Journal of the American Academy of Dermatology|October 19, 2017
Beyond the triad: Inheritance, mucocutaneous phenotype, and mortality in a cohort of patients with dyskeratosis congenitaSuzanne C Ward, Sharon A Savage, Neelam Giri, et al.
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