Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome-Reference-Cited by-同舟云学术

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Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome

Published:2005-09-09 Issue:4 Volume:43 Page:e15-e15
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Hearle N C M

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Cited by 53 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Percutaneous Treatment of Hydatid Cysts with the Ormeci Technique;TURK J GASTROENTEROL;2024

2. Clinical and Molecular Analysis in Patients with Peutz-Jeghers Syndrome;TURK J GASTROENTEROL;2024

3. GASTROINTESTINAL CANCER SYNDROMES;Counseling About Cancer;2023-03-03

4. STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome;Cureus;2023-02-01

Locally Advanced Pancreatic Ductal Adenocarcinoma: Challenges and Progress

;OncoTargets and Therapy;2020-12

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