Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: SEC23B[original query] |
---|
Clinical and genetic features of congenital dyserythropoietic anemia (CDA). European journal of haematology 2018 6 101 (3): 368-378. Moreno-Carralero María-Isabel, Horta-Herrera Saul, Morado-Arias Marta, Ricard-Andrés María-Pilar, Lemes-Castellano Angelina, Abio-Calvete Mariola, Cedena-Romero María-Teresa, González-Fernández Fernando-Ataulfo, Llorente-González Laura, Periago-Peralta Adela-María, de-la-Iglesia-Íñigo Silvia, Méndez Manuel, Morán-Jiménez María-Jo |
Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias. American journal of hematology 2018 2 93 (5): 672-682. Russo Roberta, Andolfo Immacolata, Manna Francesco, Gambale Antonella, Marra Roberta, Rosato Barbara Eleni, Caforio Paola, Pinto Valeria, Pignataro Piero, Radhakrishnan Kottayam, Unal Sule, Tomaiuolo Giovanna, Forni Gian Luca, Iolascon Achil |
Compound heterozygosity for two novel mutations of the SEC23B gene in congenital dyserythropoietic anemia type II. International journal of hematology 2021 4 114 (3): 390-394. Chen Shanshan, Guo Ziwen, Ye Yongbin, Yang Shanhong, Huang Guini |
Genetic predisposition to differentiated thyroid cancer among Polish population. Polish archives of internal medicine 2024 1 . Martyna Borowczyk, Mateusz Sypniewski, Joanna Szyda, Ma?gorzata Braszka, Katarzyna Ziemnicka, Marek Rucha?a, Michalina Oszywa, Zbigniew J Król, Paula Dobo |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
- Content source: