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Surveillance for Wilms tumour in at-risk children: pragmatic recommendations for best practice. [electronic resource] by
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- Maher, E
- Owens, C M
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- Rahman, N
Producer: 20061207
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Using Technology to Improve Adherence to HIV Medications in Transitional Age Youth: Research Reviewed, Methods Tried, Lessons Learned. [electronic resource] by
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- Mueller, M
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- Killeen, T
- Maher, E
- Drayton, C
- Dixon, T C
- Fowler, S L
- Treiber, F
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Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome. [electronic resource] by
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- Smallwood, A V
- Joyce, J A
- Murrell, A
- Lam, W
- Tang, T
- Munroe, D
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- Schofield, P N
- Maher, E R
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In:
Journal of medical genetics vol. 37
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Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markers. [electronic resource] by
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- Payne, S J
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- Richards, F M
- Chiano, M
- Hosoe, S
- Yates, J R
- Linehan, M
- Barton, D E
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Journal of medical genetics vol. 29
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326.
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Mapping of von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysis. [electronic resource] by
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- Yates, J R
- Barton, D
- Jennings, A
- Fellows, I W
- Ponder, M A
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- Benjamin, C
- Harris, R
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327.
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SLIT2 promoter methylation analysis in neuroblastoma, Wilms' tumour and renal cell carcinoma. [electronic resource] by
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- Gentle, D
- Martinsson, T
- Kogner, P
- Grundy, R
- Kishida, T
- Yao, M
- Latif, F
- Maher, E R
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British journal of cancer vol. 90
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Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor gene. [electronic resource] by
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- Tory, K
- Lush, M
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- Gustavson, K H
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In:
Journal of medical genetics vol. 30
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330.
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Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation. [electronic resource] by
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- Ohishi, S
- Mukai, T
- Joyce, J A
- Cole, T R
- Donnai, D
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- Maher, E R
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Assisted reproductive therapies and imprinting disorders--a preliminary British survey. [electronic resource] by
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- Temple, K
- Reardon, W
- Wilson, L
- Clayton-Smith, J
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- Bannister, W
- Maher, E R
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In:
Human reproduction (Oxford, England) vol. 21
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Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locus. [electronic resource] by
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- Maher, E R
- Jones, M H
- Richards, F M
- Latif, F
- Phipps, M E
- Lush, M
- Foster, K
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- Green, J S
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In:
Human molecular genetics vol. 2
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Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening. [electronic resource] by
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- Shenton, A
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- Iddenden, R
- Woodward, E R
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- Maher, E R
- Evans, D G R
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Genome-wide DNA methylation profiling of recurrent and non-recurrent chordomas. [electronic resource] by
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- Bauer, J
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- Niada, S
- Slater, A
- Gentle, D
- Maher, E R
- Jeys, L
- Grimer, R
- Sumathi, V P
- Latif, F
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In:
Epigenetics vol. 10
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337.
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Evaluation of molecular genetic diagnosis in the management of familial adenomatous polyposis coli: a population based study. [electronic resource] by
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- Barton, D E
- Slatter, R
- Koch, D J
- Jones, M H
- Nagase, H
- Payne, S J
- Charles, S J
- Moore, A T
- Nakamura, Y
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In:
Journal of medical genetics vol. 30
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338.
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Epigenetic analysis of HIC1, CASP8, FLIP, TSP1, DCR1, DCR2, DR4, DR5, KvDMR1, H19 and preferential 11p15.5 maternal-allele loss in von Hippel-Lindau and sporadic phaeochromocytomas. [electronic resource] by
- Margetts, C D E
- Astuti, D
- Gentle, D C
- Cooper, W N
- Cascon, A
- Catchpoole, D
- Robledo, M
- Neumann, H P H
- Latif, F
- Maher, E R
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In:
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Molecular genetic investigation of sporadic renal cell carcinoma: analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22. [electronic resource] by
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- Crossey, P A
- Cairns, P
- Hetherington, J W
- Richards, F M
- Jones, M H
- Bentley, E
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- Maher, E R
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In:
British journal of cancer vol. 69
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340.
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RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours. [electronic resource] by
- Astuti, D
- Agathanggelou, A
- Honorio, S
- Dallol, A
- Martinsson, T
- Kogner, P
- Cummins, C
- Neumann, H P
- Voutilainen, R
- Dahia, P
- Eng, C
- Maher, E R
- Latif, F
Producer: 20011207
In:
Oncogene vol. 20
Availability: No items available.
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