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Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33. [electronic resource] by
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Genetic steps to organ laterality in zebrafish. [electronic resource] by
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Allelic loss in esophageal squamous cell carcinoma patients with and without family history of upper gastrointestinal tract cancer. [electronic resource] by
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- Ding, T
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Guidelines for the management of postoperative soiling in children with Hirschsprung disease. [electronic resource] by
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Allelic loss on chromosome bands 13q11-q13 in esophageal squamous cell carcinoma. [electronic resource] by
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- Huang, J
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High frequency allelic loss on chromosome 17p13.3-p11.1 in esophageal squamous cell carcinomas from a high incidence area in northern China. [electronic resource] by
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Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: evidence for common founders and independent mutations. [electronic resource] by
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Familial and sporadic cases of nasopharyngeal carcinoma in Taiwan. [electronic resource] by
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Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma. [electronic resource] by
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Frequent inactivation of the TP53 gene in esophageal squamous cell carcinoma from a high-risk population in China. [electronic resource] by
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- Wang, Q H
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Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese population. [electronic resource] by
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- Ding, T
- Zhuang, Z P
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- Roth, M J
- Dawsey, S M
- He, Li-Ji
- Cao, Shu-Fen
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Allelic imbalance, including deletion of PTEN/MMACI, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutation. [electronic resource] by
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- Goldstein, A M
- Hodgson, S V
- Richardson, A L
- Robinson, B G
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Prevention of antibiotic-associated metabolic syndrome in mice by intestinal alkaline phosphatase. [electronic resource] by
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- Moaven, O
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Epstein-Barr virus microRNAs and lung cancer. [electronic resource] by
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- Roy, D
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- Linnoila, I
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CDKN2A mutations and melanoma risk in the Icelandic population. [electronic resource] by
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- Thorisdottir, K
- Ragnarsson, R
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- Kostic, J
- Masson, G
- Kristjansson, K
- Gulcher, J R
- Kong, A
- Thorsteinsdottir, U
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In:
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Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. [electronic resource] by
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- Shanley, S
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- Unden, A B
- Gillies, S
- Negus, K
- Smyth, I
- Pressman, C
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- Gerrard, B
- Goldstein, A M
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In:
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Associations of pigmentary and naevus phenotype with melanoma risk in two populations with comparable ancestry but contrasting levels of ambient sun exposure. [electronic resource] by
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- Schmid, H
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- Giles, G G
- Demenais, F
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- Elder, D E
- Mann, G J
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In:
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Localization of the gene for Cowden disease to chromosome 10q22-23. [electronic resource] by
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- Frants, R R
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- Easton, D F
- Eeles, R A
- Hodgsen, S
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- Murday, V A
- Tucker, M A
- Mariman, E C
- Starink, T M
- Ponder, B A
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- Kremer, H
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In:
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Common genetic variants in the 9p21 region and their associations with multiple tumours. [electronic resource] by
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- Berndt, S
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- Toro, J
- Mirabello, L
- Greene, M H
- Freedman, N D
- Abnet, C C
- Dawsey, S M
- Hu, N
- Qiao, Y-L
- Ding, T
- Brenner, A V
- Garcia-Closas, M
- Hayes, R
- Brinton, L A
- Lissowska, J
- Wentzensen, N
- Kratz, C
- Moore, L E
- Ziegler, R G
- Chow, W-H
- Savage, S A
- Burdette, L
- Yeager, M
- Chanock, S J
- Chatterjee, N
- Tucker, M A
- Goldstein, A M
- Yang, X R
Producer: 20130528
In:
British journal of cancer vol. 108
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