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Cited by in CrossRef
For: Jiang LX, Chen YR, Xu ZX, Zhang YH, Zhang Z, Yu PF, Dong ZW, Yang HR, Gu GL. Peutz-Jeghers syndrome without STK11 mutation may correlate with less severe clinical manifestations in Chinese patients. World J Gastroenterol 2023; 29(21): 3302-3317 [PMID: 37377590 DOI: 10.3748/wjg.v29.i21.3302]
URL: https://www.wjgnet.com/1007-9327/full/v29/i21/3302.htm
Number Citing Articles
1
Mustafa Yilmaz, Ogun Bebek, Yavuzhan Colak, Ayberk Türkyılmaz. Somatic STK11 mosaicism in a Turkish patient with Peutz-Jeghers syndromeFamilial Cancer 2024; 23(4): 641 doi: 10.1007/s10689-024-00405-z
2
Anne Marie Jelsig, John Gásdal Karstensen, Thomas V. Overeem Hansen. Progress report: Peutz–Jeghers syndromeFamilial Cancer 2024; 23(4): 409 doi: 10.1007/s10689-024-00362-7
3
Myrto Skafida, Melani M Duvall, Kristin Zelley, Sarah E. Baldino, Garrett M Brodeur, Thomas Kolon, Sogol Mostoufi‐Moab, Suzanne P. MacFarland. Conservative management of gynecomastia in Peutz‐Jeghers syndrome: Case series and review of the literaturePediatric Blood & Cancer 2024; 71(10) doi: 10.1002/pbc.31180