Peutz-Jeghers syndrome: early clinical expression of a new STK11 gene variant.

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Asymptomatic Gastric Giant Polyp in a Boy with Peutz-Jeghers Syndrome Presented with Multiple Café Au Lait Traits

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Peutz-Jeghers syndrome: early clinical expression of a new STK11 gene variant.

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Peutz-Jeghers syndrome: early clinical expression of a new STK11 gene variant.

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Peutz-Jeghers syndrome: early clinical expression of a new STK11 gene variant.

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Peutz-Jeghers syndrome: early clinical expression of a new STK11 gene variant.

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Peutz-Jeghers syndrome: early clinical expression of a new STK11 gene variant.

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Ana Isabel Lopes

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Juliette Dupont

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Marta Póvoas

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Sara Brito

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High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients.

Association of Peutz-Jeghers-like mucocutaneous pigmentation with breast and gynecologic carcinomas in women.

Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma

Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome.

Genotype-phenotype correlations in Peutz-Jeghers syndrome

High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome.

Findings from the Peutz-Jeghers syndrome registry of uruguay.

Peutz-Jeghers syndrome: a systematic review and recommendations for management.

STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.

Truncating mutations in Peutz-Jeghers syndrome are associated with more polyps, surgical interventions and cancers.

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scholarly article

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10.1136/BCR-2015-211345

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2015

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2015-10-01T00:00:00Z

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26430231

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Peutz-Jeghers syndrome: early clinical expression of a new STK11 gene variant.

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P2860

P2860

Peutz-Jeghers syndrome: early clinical expression of a new STK11 gene variant.

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P1433

P1476

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