HuGE Literature Finder
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| First Genotype-Phenotype Study in TBX4 Syndrome: Gain-of-Function Mutations Causative for Lung Disease. American journal of respiratory and critical care medicine 2022 7 206 (12): 1522-1533. Prapa Matina, Lago-Docampo Mauro, Swietlik Emilia M, Montani David, Eyries Mélanie, Humbert Marc, Welch Carrie L, Chung Wendy K, Berger Rolf M F, Bogaard Harm Jan, Danhaive Olivier, Escribano-Subías Pilar, Gall Henning, Girerd Barbara, Hernandez-Gonzalez Ignacio, Holden Simon, Hunt David, Jansen Samara M A, Kerstjens-Frederikse Wilhelmina, Kiely David G, Lapunzina Pablo, McDermott John, Moledina Shahin, Pepke-Zaba Joanna, Polwarth Gary J, Schotte Gwen, Tenorio-Castaño Jair, Thompson A A Roger, Wharton John, Wort Stephen J, Megy Karyn, Mapeta Rutendo, Treacy Carmen M, Martin Jennifer M, Li Wei, Swift Andrew J, Upton Paul D, Morrell Nicholas W, Gräf Stefan, Valverde Diana, , , |
| The determinants of survival among adults with cystic fibrosis-a cohort study. Journal of physiological anthropology 2021 11 40 (1): 19. Durda-Masny Magdalena, Go?dzik-Spychalska Joanna, John Aleksandra, Czai?ski Wojciech, Stró?ewska Weronika, Paw?owska Natalia, Wliz?o Jolanta, Batura-Gabryel Halina, Szwed Ani |
| Physical fitness and dementia risk in the very old: a study of the Lothian Birth Cohort 1921. BMC psychiatry 2018 9 18 (1): 285. Sibbett Ruth A, Russ Tom C, Allerhand Mike, Deary Ian J, Starr John |
| Association of TNF-a -308G/A, SP-B 1580 C/T, IL-13 -1055 C/T gene polymorphisms and latent adenoviral infection with chronic obstructive pulmonary disease in an Egyptian population. Archives of medical science : AMS 2012 May 8 (2): 286-95. Ezzeldin Nada, Shalaby Alaa, Saad-Hussein Amal, Ezzeldin Howayda, El Lebedy Dalia, Farouk Hebatallah, Kandil Dina |
| Serotonin-related FEV gene variant in the sudden infant death syndrome is a common polymorphism in the African-American population. Pediatric research 2009 Dec 66 (6): 631-5. Broadbelt Kevin G, Barger Melissa A, Paterson David S, Holm Ingrid A, Haas Elisabeth A, Krous Henry F, Kinney Hannah C, Markianos Kyriacos, Beggs Alan |
| Sudden infant death syndrome: rare mutation in the serotonin system FEV gene. Pediatric research 2007 Aug 62 (2): 180-2. Rand Casey M, Berry-Kravis Elizabeth M, Zhou Lili, Fan Wenqing, Weese-Mayer Debra |
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