Human Genome Epidemiology Literature Finder
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Records 1 - 2 (of 2 Records) |
| Query Trace: Death and FOXF1[original query] |
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| The OSR1 rs12329305 polymorphism contributes to the development of congenital malformations in cases of stillborn/neonatal death. Medical science monitor : international medical journal of experimental and clinical research 2014 20 1531-8. Lozi? Bernarda, Krželj Vjekoslav, Kuzmi?-Prusac Ivana, Kuzmani?-Šamija Radenka, ?apkun Vesna, Lasan Ružica, Zemunik Tatija |
| 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 |
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