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E R Maher

Showing results (121-130 of 171) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|September 16, 1999
Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutationsE M Duerr, O Gimm, D S Neuberg, et al.
Journal of the Neurological Sciences|December 1, 1990
Mapping of von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysisE R Maher, E Bentley, J R Yates, et al.
Journal of Medical Genetics|February 1, 1993
Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor geneF M Richards, E R Maher, F Latif, et al.
British Journal of Cancer|January 22, 2004
SLIT2 promoter methylation analysis in neuroblastoma, Wilms' tumour and renal cell carcinomaD Astuti, N F Da Silva, A Dallol, et al.
Journal of Medical Genetics|December 1, 1992
Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markersE R Maher, E Bentley, S J Payne, et al.
Human Reproduction (Oxford, England)|December 20, 2005
Assisted reproductive therapies and imprinting disorders--a preliminary British surveyA G Sutcliffe, C J Peters, S Bowdin, et al.
Journal of Medical Genetics|July 29, 1999
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationW W Lam, I Hatada, S Ohishi, et al.
Human Molecular Genetics|March 11, 1999
Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancerF M Richards, S A McKee, M H Rajpar, et al.
Human Molecular Genetics|March 1, 1993
Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locusP A Crossey, E R Maher, M H Jones, et al.
Journal of Medical Genetics|November 3, 2006
Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screeningA Smith, A Moran, M C Boyd, et al.
Pageof 18

Showing results (121-130 of 171) with videos related to

Sort By:
Pageof 18
The Journal of Clinical Endocrinology and Metabolism|September 16, 1999
Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutationsE M Duerr, O Gimm, D S Neuberg, et al.
Journal of the Neurological Sciences|December 1, 1990
Mapping of von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysisE R Maher, E Bentley, J R Yates, et al.
Journal of Medical Genetics|February 1, 1993
Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor geneF M Richards, E R Maher, F Latif, et al.
British Journal of Cancer|January 22, 2004
SLIT2 promoter methylation analysis in neuroblastoma, Wilms' tumour and renal cell carcinomaD Astuti, N F Da Silva, A Dallol, et al.
Journal of Medical Genetics|December 1, 1992
Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markersE R Maher, E Bentley, S J Payne, et al.
Human Reproduction (Oxford, England)|December 20, 2005
Assisted reproductive therapies and imprinting disorders--a preliminary British surveyA G Sutcliffe, C J Peters, S Bowdin, et al.
Journal of Medical Genetics|July 29, 1999
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationW W Lam, I Hatada, S Ohishi, et al.
Human Molecular Genetics|March 11, 1999
Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancerF M Richards, S A McKee, M H Rajpar, et al.
Human Molecular Genetics|March 1, 1993
Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locusP A Crossey, E R Maher, M H Jones, et al.
Journal of Medical Genetics|November 3, 2006
Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screeningA Smith, A Moran, M C Boyd, et al.
Pageof 18