Research graph
References from Endocrine manifestations of Luscan–Lumish syndrome associated with a novel SETD2 frameshift variant. Local targets link to admitted publications; unresolved targets remain external evidence.
Clinical heterogeneity in patients with SETD2 variants
10.3390/genes14061179 · 2023 · External reference
Unresolved reference
2022 · External reference
SETD2-related overgrowth syndrome
10.1002/ajmg.c.31746 · 2019 · External reference
Standards and guidelines for the interpretation of sequence variants
10.1038/gim.2015.30 · 2015 · External reference
SETD2: a role in cancer and beyond
2017 · External reference
Bariatric surgery in genetic obesity
10.1007/s11892-020-01327-7 · 2020 · External reference
Functional hypothalamic amenorrhea guideline
10.1210/jc.2017-00131 · 2017 · External reference
Hirsutism guideline
10.1210/jc.2018-00241 · 2018 · External reference
Prolactinomas
10.1016/s2213-8587(25)00227-x · 2025 · External reference
Epigenotype–phenotype correlations in SETD2 disorders
10.1093/hmg/ddad079 · 2023 · External reference
Enhanced growth hormone signaling in Luscan–Lumish syndrome
10.1210/clinem/dgaa893 · 2021 · External reference
Approach to hypogonadotropic hypogonadism
10.1210/jc.2012-3550 · 2013 · External reference
