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Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresia.
scientific article published on 21 April 2015
Author/s
author: Christopher M Grochowski, Ramakrishnan Rajagopalan, Marcella Devoto, Ellen Tsai, Nancy B Spinner, Kathleen M Loomes, Alexandra M Falsey, Ian D Krantz
Work details
Publication date
April 21, 2015
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Language
English
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