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Haematologica|October 12, 2014
Telomere length in inherited bone marrow failure syndromesBlanche P Alter, Neelam Giri, Sharon A Savage, et al.Haematologica|April 14, 2022
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohortBurak Altintas, Neelam Giri, Lisa J McReynolds, et al.Pediatric Blood & Cancer|August 13, 2017
Pregnancy outcomes in mothers of offspring with inherited bone marrow failure syndromesNeelam Giri, Helen D Reed, Pamela Stratton, et al.Aging|November 30, 2010
Telomere length in blood, buccal cells, and fibroblasts from patients with inherited bone marrow failure syndromesShahinaz M Gadalla, Richard Cawthon, Neelam Giri, et al.Vaccine|December 4, 2013
Antibody response to human papillomavirus vaccine in subjects with inherited bone marrow failure syndromesBlanche P Alter, Neelam Giri, Yuanji Pan, et al.Cancer Genetics|October 23, 2021
Genotype-cancer association in patients with Fanconi anemia due to pathogenic variants in FANCD1 (BRCA2) or FANCN (PALB2)Lisa J McReynolds, Kajal Biswas, Neelam Giri, et al.The Journal of Clinical Endocrinology and Metabolism|January 21, 2014
Anti-Müllerian hormone deficiency in females with Fanconi anemiaMartha M Sklavos, Neelam Giri, Pamela Stratton, et al.Journal of the American Academy of Dermatology|October 17, 2017
Progressive reticulate skin pigmentation and anonychia in a patient with bone marrow failureSuzanne C Ward, Sharon A Savage, Neelam Giri, et al.British Journal of Haematology|March 27, 2014
Response to androgen therapy in patients with dyskeratosis congenitaPayal P Khincha, Ingrid M Wentzensen, Neelam Giri, et al.The Journal of Hand Surgery, European Volume|April 1, 2022
The incidence and spectrum of congenital hand differences in patients with Fanconi anaemia: analysis of 48 patientsGrainne Bourke, Daniel Wilks, Sally Kinsey, et al.Pageof 10