Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and KLLN[original query] |
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Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations. The Journal of clinical endocrinology and metabolism 2011 Dec 96 (12): E2063-71. Ngeow Joanne, Mester Jessica, Rybicki Lisa A, Ni Ying, Milas Mira, Eng Char |
KLLN epigenotype-phenotype associations in Cowden syndrome. European journal of human genetics : EJHG 2015 Feb . Nizialek Emily A, Mester Jessica L, Dhiman Vineet K, Smiraglia Dominic J, Eng Char |
Circulating levels of PTEN and KLLN in papillary thyroid carcinoma: can they be considered as novel diagnostic biomarkers? Endocrine 2017 7 57 (3): 428-435. Razavi S Adeleh, Modarressi Mohammad Hossein, Yaghmaei Parichehr, Tavangar S Mohammad, Hedayati Meh |
Looking for the hidden mutation: Bannayan-Riley-Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A. American journal of medical genetics. Part A 2019 May . Golas Monika M, Auber Bernd, Ripperger Tim, Pabst Brigitte, Schmidt Gunnar, Morlot Michel, Diebold Uta, Steinemann Doris, Schlegelberger Brigitte, Morlot Susan |
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