Showing results (351-360 of 628) with videos related to
Sort By:
Pageof 63
American Journal of Medical Genetics. Part A|November 3, 2007
Mapping of a novel type III variant of Knobloch syndrome (KNO3) to chromosome 17q11.2Shagufta Khaliq, Aiysha Abid, Dominick R A White, 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.ASAIO Journal (American Society for Artificial Internal Organs : 1992)|July 1, 1992
Development of an axial flow blood pump LVASK C Butler, T R Maher, H S Borovetz, 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.The Journal of Clinical Endocrinology and Metabolism|January 10, 2026
Expanding the clinical tumor phenotype of the EPAS1-asssociated tumor syndromeYasemin Cole, Sophie Howarth, Asna Javaid, 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.Epigenetics|July 27, 2013
RASSF2 methylation is a strong prognostic marker in younger age patients with Ewing sarcomaSeley Gharanei, Anna T Brini, Sumathi Vaiyapuri, et al.Molecular Cancer|July 3, 2009
The novel RASSF6 and RASSF10 candidate tumour suppressor genes are frequently epigenetically inactivated in childhood leukaemiasLuke B Hesson, Thomas L Dunwell, Wendy N Cooper, et al.Cardiovascular Research|October 5, 2010
The role of vascular myoglobin in nitrite-mediated blood vessel relaxationJulian O M Ormerod, Houman Ashrafian, Abdul R Maher, et al.Pageof 63