Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Hypertension and FOXF1[original query] |
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Genetic basis for childhood interstitial lung disease among Japanese infants and children. Pediatric research 2018 3 83 (2): 477-483. Hayasaka Itaru, Cho Kazutoshi, Akimoto Takuma, Ikeda Masahiko, Uzuki Yutaka, Yamada Masafumi, Nakata Koh, Furuta Itsuko, Ariga Tadashi, Minakami Hisano |
Alveolar capillary dysplasia with misalignment of the pulmonary veins and hypoplastic left heart sequence caused by an in frame deletion within FOXF1. American journal of medical genetics. Part A 2019 5 179 (7): 1325-1329. Bourque Danielle K, Fonseca Inara Chacon, Staines Andrea, Teitelbaum Ronni, Axford Michelle M, Jobling Rebekah, Chiasson David, Chitayat Dav |
Incidence of alveolar capillary dysplasia with misalignment of pulmonary veins in infants with unexplained severe pulmonary hypertension: The roles of clinical, pathological, and genetic testing. Early human development 2021 Jan 155 105323. Onda Tetsuo, Akimoto Takuma, Hayasaka Itaru, Ikeda Masahiko, Furuse Yuta, Ando Akiko, Nakamura Yuichi, Honjo Ryota, Manabe Atsushi, Furuta Itsuko, Cho Kazutos |
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- Page last updated:Mar 25, 2024
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