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Identification of the molecular etiology in rare congenital hemolytic anemias using next‐generation sequencing with exome‐based copy number variant analysis.

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Title: Identification of the molecular etiology in rare congenital hemolytic anemias using next‐generation sequencing with exome‐based copy number variant analysis.
Authors: Isik, Esra1 (AUTHOR) esrabadak36@gmail.com, Aydinok, Yesim2 (AUTHOR), Albayrak, Canan3 (AUTHOR), Durmus, Basak1 (AUTHOR), Karakas, Zeynep4 (AUTHOR), Orhan, Mehmet Fatih5 (AUTHOR), Sarper, Nazan6 (AUTHOR), Aydın, Sultan7 (AUTHOR), Unal, Selma8 (AUTHOR), Oymak, Yesim9 (AUTHOR), Karadas, Nihal1 (AUTHOR), Turedi, Aysen10 (AUTHOR), Albayrak, Davut11 (AUTHOR), Tayfun, Funda12 (AUTHOR), Tugcu, Deniz4 (AUTHOR), Karaman, Serap4 (AUTHOR), Tobu, Mahmut13 (AUTHOR), Unal, Ekrem14 (AUTHOR), Ozcan, Alper14 (AUTHOR), Unal, Sule15 (AUTHOR)
Source: European Journal of Haematology. Jul2024, Vol. 113 Issue 1, p82-89. 8p.
Database: Academic Search Ultimate
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  Data: Identification of the molecular etiology in rare congenital hemolytic anemias using next‐generation sequencing with exome‐based copy number variant analysis.
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  Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Haematology%22">European Journal of Haematology</searchLink>. Jul2024, Vol. 113 Issue 1, p82-89. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=177627291
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        Text: English
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              Text: Jul2024
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