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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 27, 2016
Von Hippel-Lindau Disease: Genetics and Role of Genetic Counseling in a Multiple Neoplasia SyndromeSarah M Nielsen, Lindsay Rhodes, Ignacio Blanco, et al.Trends in Molecular Medicine|September 29, 2014
CDKN1C mutations: two sides of the same coinThomas Eggermann, Gerhard Binder, Frédéric Brioude, et al.The Lancet. Global Health|January 31, 2025
The prevalence of hypoxaemia in paediatric and adult patients in health-care facilities in low-income and middle-income countries: a systematic review and meta-analysisHamish R Graham, Esrat Jahan, Rami Subhi, et al.Systematic Reviews|September 4, 2016
A systematic review of St. John's wort for major depressive disorderEric A Apaydin, Alicia R Maher, Roberta Shanman, et al.Journal of Medical Genetics|January 11, 2000
Epigenotype-phenotype correlations in Beckwith-Wiedemann syndromeJ R Engel, A Smallwood, A Harper, et al.Journal of Medical Genetics|November 1, 1995
Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytomaP A Crossey, C Eng, M Ginalska-Malinowska, et al.Journal of Medical Genetics|February 28, 2018
Penetrance estimates for BRCA1, BRCA2 (also applied to Lynch syndrome) based on presymptomatic testing: a new unbiased method to assess risk?D Gareth Evans, Emma Woodward, Elaine F Harkness, et al.Breast Cancer Research : BCR|December 26, 2006
Parity and breast cancer risk among BRCA1 and BRCA2 mutation carriersAntonis C Antoniou, Andrew Shenton, Eamonn R Maher, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|May 27, 2014
An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesisHakan Cangul, Halil Saglam, Yaman Saglam, et al.European Journal of Haematology|September 24, 2024
Clonal Evolution in 207 Cases of Refractory or Relapsed Acute Myeloid LeukemiaGraeme F Murray, Ian M Bouligny, Thuy Ho, et al.Pageof 63