STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome.

Chiraphapphaiboon, Wannasiri; Thongnoppakhun, Wanna; Limjindaporn, Thawornchai; Sawasdichai, Sunisa; Roothumnong, Ekkapong; Prangphan, Kanjana; Pamornpol, Benjaporn; Limwongse, Chanin; Pithukpakorn, Manop

Chiraphapphaiboon, Wannasiri; Thongnoppakhun, Wanna; Limjindaporn, Thawornchai; Sawasdichai, Sunisa; Roothumnong, Ekkapong; Prangphan, Kanjana; Pamornpol, Benjaporn; Limwongse, Chanin; Pithukpakorn, Manop.

Afiliação

Chiraphapphaiboon W; Department of Anatomy, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Thongnoppakhun W; Siriraj Genomics, Office of the Dean, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Limjindaporn T; Department of Anatomy, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Sawasdichai S; Siriraj Genomics, Office of the Dean, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Roothumnong E; Division of Medical Genetics, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Prangphan K; Siriraj Genomics, Office of the Dean, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Pamornpol B; Department of Anatomy, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Limwongse C; Siriraj Genomics, Office of the Dean, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.
Pithukpakorn M; Division of Medical Genetics, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, THA.

Cureus ; 15(2): e34495, 2023 Feb.

Article em En | MEDLINE | ID: mdl-36874343

Palavras-chave

copy number variations; deletions; mutations; peutz-jeghers syndrome; stk11

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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Cureus Ano de publicação: 2023 Tipo de documento: Article