Inherited bone marrow failure syndromes: considerations pre- and posttransplant von Alter, Blanche P.

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Holographic three-dimensional telepresence using large-area photorefractive polymer von Peyghambarian, N, Blanche, P.-A, Bablumian, A, Voorakaranam, R, Christenson, C, Lin, W, Gu, T, Flores, D, Wang, P, Hsieh, W.-Y, Kathaperumal, M, Rachwal, B, Siddiqui, O, Thomas, J, Norwood, R. A, Yamamoto, M

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Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up von Alter, Blanche P, Giri, Neelam, Savage, Sharon A, Rosenberg, Philip S

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Fanconi anemia and the development of leukemia von Alter, Blanche P., MD, MPH

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Pathophysiology and management of inherited bone marrow failure syndromes von Shimamura, Akiko, Alter, Blanche P

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Inherited bone marrow failure syndromes: considerations pre- and posttransplant von Alter, Blanche P

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An updatable holographic three-dimensional display von Tay, Sava, Peyghambarian, N, Blanche, P.-A, Voorakaranam, R, Tunç, A. V, Lin, W, Rokutanda, S, Gu, T, Flores, D, Wang, P, Li, G, St Hilaire, P, Thomas, J, Norwood, R. A, Yamamoto, M

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Incidence of neoplasia in Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry von Vlachos, Adrianna, Rosenberg, Philip S., Atsidaftos, Eva, Alter, Blanche P., Lipton, Jeffrey M.

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TINF2, a Component of the Shelterin Telomere Protection Complex, Is Mutated in Dyskeratosis Congenita von Savage, Sharon A., Giri, Neelam, Baerlocher, Gabriela M., Orr, Nick, Lansdorp, Peter M., Alter, Blanche P.

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Cancer in dyskeratosis congenita von Alter, Blanche P., Giri, Neelam, Savage, Sharon A., Rosenberg, Philip S.

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Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort von Altintas, Burak, Giri, Neelam, McReynolds, Lisa J, Best, Ana, Alter, Blanche P

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Increased risk of colon cancer and osteogenic sarcoma in Diamond-Blackfan anemia von Vlachos, Adrianna, Rosenberg, Philip S., Atsidaftos, Eva, Kang, Jessica, Onel, Kenan, Sharaf, Ravi N., Alter, Blanche P., Lipton, Jeffrey M.

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Diagnosis, genetics, and management of inherited bone marrow failure syndromes von Alter, Blanche P

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Thinking of VACTERL-H? Rule out Fanconi Anemia according to PHENOS von Alter, Blanche P., Giri, Neelam

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Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita von Ballew, Bari J., Yeager, Meredith, Jacobs, Kevin, Giri, Neelam, Boland, Joseph, Burdett, Laurie, Alter, Blanche P., Savage, Sharon A.

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Disease progression and clinical outcomes in telomere biology disorders von Niewisch, Marena R., Giri, Neelam, McReynolds, Lisa J., Alsaggaf, Rotana, Bhala, Sonia, Alter, Blanche P., Savage, Sharon A.

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Cancer in Fanconi anemia, 1927–2001 von Alter, Blanche P.

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Fanconi anaemia: A syndrome with distinct subgroups von Alter, Blanche P., Giri, Neelam, McReynolds, Lisa J., Altintas, Burak

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Disruption of telomerase trafficking by TCAB1 mutation causes dyskeratosis congenita von Zhong, Franklin, Savage, Sharon A, Shkreli, Marina, Giri, Neelam, Jessop, Lea, Myers, Timothy, Chen, Renee, Alter, Blanche P, Artandi, Steven E

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Telomere length is associated with disease severity and declines with age in dyskeratosis congenita von ALTER, Blanche P, ROSENBERG, Philip S, GIRI, Neelam, BAERLOCHER, Gabriela M, LANSDORP, Peter M, SAVAGE, Sharon A

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