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American Journal of Medical Genetics. Part A|September 16, 2024
Germline RTEL1 Variants in Telomere Biology DisordersAshley S Thompson, Marena R Niewisch, Neelam Giri, et al.Familial Cancer|June 21, 2024
Benign tumors and non-melanoma skin cancers in patients with Fanconi anemiaAura Enache, Bia Sajjad, Burak Altintas, et al.American Journal of Medical Genetics. Part A|October 3, 2008
All in the family: disclosure of "unwanted" information to an adolescent to benefit a relativeColleen C Denny, Benjamin S Wilfond, June A Peters, et al.Blood Reviews|July 29, 2019
Genotype-phenotype associations in Fanconi anemia: A literature reviewMoisés O Fiesco-Roa, Neelam Giri, Lisa J McReynolds, et al.Ophthalmology|December 22, 2009
Ocular and orbital manifestations of the inherited bone marrow failure syndromes: Fanconi anemia and dyskeratosis congenitaEkaterini T Tsilou, Neelam Giri, Sarah Weinstein, et al.JAMA Network Open|December 11, 2024
Genotype and Associated Cancer Risk in Individuals With Telomere Biology DisordersMarena R Niewisch, Jung Kim, Neelam Giri, et al.The Journal of Clinical Endocrinology and Metabolism|November 19, 2014
Reduced serum levels of anti-Müllerian hormone in females with inherited bone marrow failure syndromesMartha M Sklavos, Pamela Stratton, Neelam Giri, et al.Cytogenetic and Genome Research|September 18, 2014
Comparison of chromosome breakage in non-mosaic and mosaic patients with Fanconi anemia, relatives, and patients with other inherited bone marrow failure syndromesJohn H Fargo, Andrzej Rochowski, Neelam Giri, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Risk of cancer in heterozygous relatives of patients with Fanconi anemiaLisa J McReynolds, Neelam Giri, Lisa Leathwood, et al.Journal of Medical Genetics|January 7, 2011
Sequence analysis of the shelterin telomere protection complex genes in dyskeratosis congenitaSharon A Savage, Neelam Giri, Lea Jessop, et al.Pageof 10