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Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans. [electronic resource] by
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- Henderson, Michael
- Yang, Lingyao
- Walsh, Kyle M
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- Wiencke, John K
- Spitz, Margaret R
- Wenzlaff, Angela S
- Wrensch, Margaret R
- Eaton, Charles B
- Furberg, Helena
- Mark Brown, W
- Goldstein, Benjamin A
- Assimes, Themistocles
- Tang, Hua
- Kooperberg, Charles L
- Quesenberry, Charles P
- Tindle, Hilary
- Patel, Manali I
- Amos, Christopher I
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Producer: 20161213
In:
EBioMedicine vol. 4
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Sickle cell screening in Uganda: High burden, human immunodeficiency virus comorbidity, and genetic modifiers. [electronic resource] by
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- McElhinney, Kathryn E
- Ndeezi, Grace
- Howard, Thad A
- Ndugwa, Christopher M
- Ware, Russell E
- Aceng, Jane R
Producer: 20200122
In:
Pediatric blood & cancer vol. 66
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Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation. [electronic resource] by
- Jiang, Pingping
- Liang, Min
- Zhang, Chaofan
- Zhao, Xiaoxu
- He, Qiufen
- Cui, Limei
- Liu, Xiaoling
- Sun, Yan-Hong
- Fu, Qun
- Ji, Yanchun
- Bai, Yidong
- Huang, Taosheng
- Guan, Min-Xin
Producer: 20170713
In:
Human molecular genetics vol. 25
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Ancestral haplotype 8.1 and lung disease severity in European cystic fibrosis patients. [electronic resource] by
- Corvol, Harriet
- Beucher, Julie
- Boëlle, Pierre-Yves
- Busson, Pierre-François
- Muselet-Charlier, Céline
- Clement, Annick
- Ratjen, Felix
- Grasemann, Hartmut
- Laki, Judith
- Palmer, Colin N A
- Elborn, J Stuart
- Mehta, Anil
Producer: 20120702
In:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society vol. 11
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155.
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The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients. [electronic resource] by
- Sanchez-Dominguez, Celia N
- Reyes-Lopez, Miguel A
- Bustamante, Adriana
- Cerda-Flores, Ricardo M
- Villalobos-Torres, Maria Del C
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- Rojas-Martinez, Augusto
- Martinez-Rodriguez, Herminia G
- Barrera-Saldaña, Hugo A
- Ortiz-Lopez, Rocio
Producer: 20150212
In:
PloS one vol. 9
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The C-terminal HCN4 variant P883R alters channel properties and acts as genetic modifier of atrial fibrillation and structural heart disease. [electronic resource] by
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- Geschwill, Pascal
- Reiss, Miriam
- Bruehl, Claus
- Draguhn, Andreas
- Koenen, Michael
- Sedaghat-Hamedani, Farbod
- Meder, Benjamin
- Thomas, Dierk
- Katus, Hugo A
- Schweizer, Patrick A
Producer: 20200526
In:
Biochemical and biophysical research communications vol. 519
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