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Fetal Diagnosis and Therapy|January 22, 2020
Exome Sequencing for Prenatal Detection of Genetic Abnormalities in Fetal Ultrasound Anomalies: An Economic EvaluationShahela S Kodabuckus, Elizabeth Quinlan-Jones, Dominic J McMullan, et al.
Journal of Clinical Pathology|October 5, 2022
Preferential MGMT hypermethylation in SDH-deficient wild-type GISTOlivier T Giger, Rogier Ten Hoopen, David Shorthouse, et al.
The British Journal of Ophthalmology|November 12, 2003
Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2)M Michaelides, I A Aligianis, G E Holder, et al.
International Journal of Cancer|March 1, 2006
Molecular genetic evidence that endometriosis is a precursor of ovarian cancerAmanda H Prowse, Sanjiv Manek, Rajesh Varma, et al.
Molecular Cancer Therapeutics|January 12, 2011
Therapeutic targeting the loss of the birt-hogg-dube suppressor geneXiaohong Lu, Wenbin Wei, Janine Fenton, et al.
Environmental Health Perspectives|October 23, 2012
Heavy metal lead exposure, osteoporotic-like phenotype in an animal model, and depression of Wnt signalingEric E Beier, Jason R Maher, Tzong-Jen Sheu, et al.
Human Reproduction (Oxford, England)|October 9, 2007
A survey of assisted reproductive technology births and imprinting disordersSarah Bowdin, Cathy Allen, Gail Kirby, et al.
Prenatal Diagnosis|December 6, 2023
When should we offer antenatal sequencing for urinary tract malformations? A systematic review, cohort study and meta-analysisSarah Sonner, Kelly Reilly, Adrian S Woolf, et al.
Oncogene|February 16, 2010
Identification of candidate tumour suppressor genes frequently methylated in renal cell carcinomaM R Morris, C Ricketts, D Gentle, et al.
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