Suchergebnisse - "McReynolds, Lisa J"

PubPharm (15)

1

Inherited bone marrow failure syndromes : a review of current practices and potential future research directions

enthalten in: Current opinion in pediatrics | 2023

von Deng, J. | McReynolds, L.

2

Genotype-phenotype and outcome associations in patients with Fanconi anemia : the National Cancer Institute cohort

enthalten in: Haematologica | 2023

von Altintas, B. | Giri, N. | McReynolds, L. | +2

3

Next-generation sequencing errors due to genetic variation in WRAP53 encoding TCAB1 on chromosome 17

enthalten in: Human mutation | 2022

von Savage, S. | Jones, K. | Teshome, K. | +3

4

Shwachman Diamond syndrome : narrow genotypic spectrum and variable clinical features

enthalten in: Pediatric research | 2022

von Thompson, A. | Giri, N. | Gianferante, D. | +4

5

Disease progression and clinical outcomes in telomere biology disorders

enthalten in: Blood | 2022

von Niewisch, M. | Giri, N. | McReynolds, L. | +4

CommentIn: Blood. 2022 Mar 24;139(12):1776-1777. - PMID 35323880

6

Genotype-cancer association in patients with Fanconi anemia due to pathogenic variants in FANCD1 (BRCA2) or FANCN (PALB2)

enthalten in: Cancer genetics | 2021

von McReynolds, L. | Biswas, K. | Giri, N. | +2

7

Prognostic impact of pre-transplant chromosomal aberrations in peripheral blood of patients undergoing unrelated donor hematopoietic cell transplant for acute myeloid leukemia

enthalten in: Scientific reports | 2021

von Wang, Y. | Zhou, W. | McReynolds, L. | +25

8

The causes of Fanconi anemia in South Asia and the Middle East : A case series and review of the literature

enthalten in: Molecular genetics & genomic medicine | 2021

von Thompson, A. | Saba, N. | McReynolds, L. | +10

9

Gastrointestinal Hemorrhage : A Manifestation of the Telomere Biology Disorders

enthalten in: The Journal of pediatrics | 2021

von Himes, R. | Chiou, E. | Queliza, K. | +22

CommentIn: J Pediatr. 2021 Mar;230:12-14. - PMID 33121962

10

Gata2 deficiency delays leukemogenesis while contributing to aggressive leukemia phenotype in Cbfb-MYH11 knockin mice

enthalten in: Leukemia | 2020

von Saida, S. | Zhen, T. | Kim, E. | +4