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Genotype-phenotype correlations in Peutz-Jeghers syndrome

Genotype-phenotype correlations in Peutz-Jeghers syndrome

http://www.wikidata.org/entity/Q34547534

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Oral pigmentation: A review A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients.Mutations in STK11 gene in Czech Peutz-Jeghers patients Spectrum of LKB1, EGFR, and KRAS mutations in chinese lung adenocarcinomas.Peutz-Jeghers syndrome with germline mutation of STK11.Lower gastrointestinal tract cancer predisposition syndromes Chemopreventive efficacy of rapamycin on Peutz-Jeghers syndrome in a mouse model.Identification of patients at risk for hereditary colorectal cancer Findings from the Peutz-Jeghers syndrome registry of uruguay.The lentiginoses: cutaneous markers of systemic disease and a window to new aspects of tumourigenesis.Q-switched Nd:YAG laser treatment for labial lentigines associated with Peutz-Jeghers syndrome.Cancer risks in LKB1 germline mutation carriers.Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndrome.A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report Diagnostic Approach to Hereditary Colorectal Cancer Syndromes.Familial Gastric Cancers.ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes Novel serine/threonine kinase 11 gene mutations in Peutz-Jeghers syndrome patients and endoscopic management Genomic Biomarkers for Breast Cancer Risk.Novel mutations in the STK11 gene in Thai patients with Peutz-Jeghers syndrome.Correlation between genotype and phenotype in three families with Peutz-Jeghers Syndrome.Small bowel polyposis syndromes.Familial colorectal cancer type X: genetic profiles and phenotypic features.Exceptional durable response to everolimus in a patient with biphenotypic breast cancer harboring an STK11 variant.A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case report.Time to incorporate germline multigene panel testing into breast and ovarian cancer patient care.STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.Identification of a novel de novo STK11 mutation in a Chinese child with Peutz-Jeghers syndrome.Disease pattern in Danish patients with Peutz-Jeghers syndrome.Peutz-Jeghers syndrome: early clinical expression of a new STK11 gene variant.Unusually early presentation of small-bowel adenocarcinoma in a patient with Peutz-Jeghers syndrome.Complete STK11 Deletion and Atypical Symptoms in Peutz-Jeghers Syndrome Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.STK11 status and intussusception risk in Peutz-Jeghers syndrome.Somatic alterations of the serine/threonine kinase LKB1 gene in squamous cell (SCC) and large cell (LCC) lung carcinoma.Phe354Leu Polymorphism of LKB1 Is a Potential Prognostic Factor for Cytogenetically Normal Acute Myeloid Leukemia.An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review.Gastrointestinal diseases and their oro-dental manifestations: Part 4: Peutz-Jeghers syndrome.Analysis of STK11 gene variant in five Chinese patients with Peutz-Jeghers syndrome.First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome.

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Genotype-phenotype correlations in Peutz-Jeghers syndrome

http://www.wikidata.org/entity/Q34547534

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Genotype-phenotype correlations in Peutz-Jeghers syndrome

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Genotype-phenotype correlations in Peutz-Jeghers syndrome

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P2860

Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity

Base-calling of automated sequencer traces using phred. II. Error probabilities

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

Consed: a graphical tool for sequence finishing

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

A randomized trial of aspirin to prevent colorectal adenomas in patients with previous colorectal cancer

LKB1--a master tumour suppressor of the small intestine and beyond

Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2

Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

The effect of celecoxib, a cyclooxygenase-2 inhibitor, in familial adenomatous polyposis

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