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European Journal of Human Genetics : EJHG|February 25, 2026
Familial pneumothorax in twins with Tatton-Brown-Rahman DNMT3A overgrowth syndromeSarju G Mehta, Simon Holden, Judith Babar, et al.
Human Mutation|May 4, 2011
Birt Hogg-Dubé syndrome-associated FLCN mutations disrupt protein stabilityMichael S Nahorski, Anne Reiman, Derek H K Lim, et al.
Nature|June 3, 1999
The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysisP H Maxwell, M S Wiesener, G W Chang, et al.
Human Reproduction (Oxford, England)|December 17, 2008
Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologiesDerek Lim, Sarah C Bowdin, Louise Tee, et al.
Oncogene|December 7, 2010
Genome-wide methylation analysis identifies epigenetically inactivated candidate tumour suppressor genes in renal cell carcinomaM R Morris, C J Ricketts, D Gentle, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 21, 2013
Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysisS C Hillman, D J McMullan, G Hall, et al.
Surgery|December 15, 2000
Clinical and genetic analysis of patients with pancreatic neuroendocrine tumors associated with von Hippel-Lindau diseaseS K Libutti, P L Choyke, H R Alexander, et al.
JAMA Oncology|December 15, 2015
Multilocus Inherited Neoplasia Alleles Syndrome: A Case Series and ReviewJames Whitworth, Anne-Bine Skytte, Lone Sunde, et al.
EJNMMI Research|October 21, 2025
In vivo gastrin releasing peptide receptor expression in SDH deficient wild-type gastrointestinal stromal tumours (GIST): potential for theranostic applicationsDavid G E Hulse, Ines Harper, Fung Tan, et al.
Oncogene|September 27, 2006
Identification of novel VHL targets that are associated with the development of renal cell carcinomaM Abdulrahman, E N Maina, M R Morris, et al.
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