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Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients

Hereditary erythrocytes disorders include a large group of conditions with heterogeneous molecular bases and phenotypes. We analyzed here a case series of 155 consecutive patients with clinical suspicion of hereditary erythrocyte defects referred to the Medical Genetics Unit from 2018 to 2020. All o...

詳細記述

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書誌詳細
出版年:Genes (Basel)
主要な著者: Andolfo, Immacolata, Martone, Stefania, Rosato, Barbara Eleni, Marra, Roberta, Gambale, Antonella, Forni, Gian Luca, Pinto, Valeria, Göransson, Magnus, Papadopoulou, Vasiliki, Gavillet, Mathilde, Elalfy, Mohsen, Panarelli, Antonella, Tomaiuolo, Giovanna, Iolascon, Achille, Russo, Roberta
フォーマット: Artigo
言語:Inglês
出版事項: MDPI 2021
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC8304671/
https://ncbi.nlm.nih.gov/pubmed/34201899
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12070958
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