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E R Maher

Showing results (81-90 of 171) with videos related to

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Human Molecular Genetics|November 1, 1995
Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease geneF M Richards, S J Payne, B Zbar, et al.
European Journal of Cancer (Oxford, England : 1990)|December 1, 1995
Molecular genetic analysis of the von Hippel-Lindau disease (VHL) tumour suppressor gene in gonadal tumoursK Foster, R J Osborne, R A Huddart, et al.
The Quarterly Journal of Medicine|November 1, 1990
Clinical features and natural history of von Hippel-Lindau diseaseE R Maher, J R Yates, R Harries, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 27, 2010
Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysisS C Hillman, S Pretlove, A Coomarasamy, et al.
Hormone Research in Paediatrics|March 2, 2010
SDHD-related chromaffin tumours: disease localisation to genetic dysfunctionU Srirangalingam, B Khoo, M Matson, et al.
Toxicology Letters|April 27, 2001
Genomic imprinting and cancer; new paradigms in the genetics of neoplasiaP N Schofield, J A Joyce, W K Lam, et al.
Familial Cancer|December 22, 2011
Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutationsA Moran, C O'Hara, S Khan, et al.
Clinical Genetics|December 1, 1995
Molecular genetic analysis of exons 1 to 6 of the APC gene in non-polyposis familial colorectal cancerJ A Joyce, N J Froggatt, R Davies, et al.
Human Molecular Genetics|September 1, 1997
Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndromeJ A Joyce, W K Lam, D J Catchpoole, et al.
Journal of Neurosurgery|May 1, 1996
Molecular genetic investigation of the neurofibromatosis type 2 tumor suppressor gene in sporadic meningiomaT Harada, R M Irving, J H Xuereb, et al.
Pageof 18

Showing results (81-90 of 171) with videos related to

Sort By:
Pageof 18
Human Molecular Genetics|November 1, 1995
Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease geneF M Richards, S J Payne, B Zbar, et al.
European Journal of Cancer (Oxford, England : 1990)|December 1, 1995
Molecular genetic analysis of the von Hippel-Lindau disease (VHL) tumour suppressor gene in gonadal tumoursK Foster, R J Osborne, R A Huddart, et al.
The Quarterly Journal of Medicine|November 1, 1990
Clinical features and natural history of von Hippel-Lindau diseaseE R Maher, J R Yates, R Harries, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 27, 2010
Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysisS C Hillman, S Pretlove, A Coomarasamy, et al.
Hormone Research in Paediatrics|March 2, 2010
SDHD-related chromaffin tumours: disease localisation to genetic dysfunctionU Srirangalingam, B Khoo, M Matson, et al.
Toxicology Letters|April 27, 2001
Genomic imprinting and cancer; new paradigms in the genetics of neoplasiaP N Schofield, J A Joyce, W K Lam, et al.
Familial Cancer|December 22, 2011
Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutationsA Moran, C O'Hara, S Khan, et al.
Clinical Genetics|December 1, 1995
Molecular genetic analysis of exons 1 to 6 of the APC gene in non-polyposis familial colorectal cancerJ A Joyce, N J Froggatt, R Davies, et al.
Human Molecular Genetics|September 1, 1997
Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndromeJ A Joyce, W K Lam, D J Catchpoole, et al.
Journal of Neurosurgery|May 1, 1996
Molecular genetic investigation of the neurofibromatosis type 2 tumor suppressor gene in sporadic meningiomaT Harada, R M Irving, J H Xuereb, et al.
Pageof 18