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Academic Journal

A novel missense mutation of the STK11 gene in a Chinese family with Peutz-Jeghers syndrome.

Subjects: *PEUTZ-Jeghers syndrome; *GENE families; *MISSENSE mutation

  • Source: BMC Gastroenterology. 12/22/2022, Vol. 22 Issue 1, p1-7. 7p.

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Academic Journal

The role of STK 11 gene testing in individuals with oral pigmentation.

Subjects: *PEUTZ-Jeghers syndrome; *PIGMENTATION disorders; *LAUGIER-Hunziker syndrome

  • Source: Australasian Journal of Dermatology. May2017, Vol. 58 Issue 2, p135-138. 4p. 1 Color Photograph.

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Academic Journal

Germline mutations of the STK11 gene in Korean Peutz–Jeghers syndrome patients.

Subjects: *PEUTZ-Jeghers syndrome; *GENETIC mutation; *PATIENTS

  • Source: British Journal of Cancer. 4/15/2000, Vol. 82 Issue 8, p1403. 4p.

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Academic Journal

A novel stop codon mutation in STK11 gene is associated with Peutz-Jeghers Syndrome and elevated cancer risk: a case study.

Subjects: BIOMARKERS; STOMACH; GENETIC mutation

  • Source: Gastroenterology & Hepatology from Bed to Bench; Summer2023, Vol. 16 Issue 3, p341-346, 6p

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Academic Journal

Lung cancer as a predominant feature in a patient with Peutz–Jeghers syndrome: Case report.

Subjects: LUNG cancer treatment; LUNG cancer diagnosis; ADENOCARCINOMA

  • Source: Thoracic Cancer; Jun2022, Vol. 13 Issue 12, p1862-1865, 4p

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Academic Journal

Early screening the small bowel is key to protect Peutz-Jeghers syndrome patients from surgery: a novel mutation c.243delG in STK11 gene.

Subjects: *PEUTZ-Jeghers syndrome; *HAMARTOMA; *GASTROINTESTINAL agents

  • Source: BMC Gastroenterology. 5/9/2019, Vol. 19 Issue 1, pN.PAG-N.PAG. 1p. 1 Color Photograph, 2 Charts.

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Academic Journal

The altered activity of P53 signaling pathway by STK11 gene mutations and its cancer phenotype in Peutz-Jeghers syndrome.

Subjects: *PEUTZ-Jeghers syndrome; *GENETIC mutation; *CANCER

  • Source: BMC Medical Genetics. 8/9/2018, Vol. 19 Issue 1, pN.PAG-N.PAG. 1p.

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Academic Journal

Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome.

Subjects: *PEUTZ-Jeghers syndrome; *GENETIC mutation; *SERINE/THREONINE kinase geneticsCHINA

  • Source: BMC Gastroenterology. 11/25/2015, Vol. 15, p1-8. 8p. 1 Color Photograph, 1 Diagram, 3 Charts, 1 Graph.

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Academic Journal

Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome.

Subjects: RNA analysis; GENETIC polymorphisms; GENETIC mutationCHINA

  • Source: BioMed Research International; 5/12/2020, p1-12, 12p

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Academic Journal

Delayed diagnosis of Peutz-Jeghers syndrome due to pathological information loss or mistake in family/personal history.

Subjects: *PEUTZ-Jeghers syndrome; *DELAYED diagnosis; *GENETIC disorder diagnosis

  • Source: Orphanet Journal of Rare Diseases. 6/8/2021, Vol. 16 Issue 1, p1-6. 6p.

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  • 1-10 of  458 results for ""PEUTZ-Jeghers syndrome""