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Article

Complete germline deletion of the STK11 gene in a family with Peutz–Jeghers syndrome

18 Feb 2004

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 14970844
DOI: 10.1038/sj.ejhg.5201155

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Complete germline deletion of the STK11 gene in a family with Peutz–Jeghers syndromePMID 14970844Read ↗

Gene symbol: STK11. Disease: Peutz-Jeghers Syndrome.Semantic proximity Read ↗

STK11 genotyping and cancer risk in Peutz-Jeghers syndromeSemantic proximity Read ↗

Haploinsufficiency of STK11 and neighboring genes cause a contiguous gene syndrome including Peutz-Jeghers phenotype.Semantic proximity Read ↗

A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients.Semantic proximity Read ↗

A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History.Semantic proximity Read ↗

STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients.Semantic proximity Read ↗

A novel mutation in STK11 gene is associated with Peutz-Jeghers syndrome in Chinese patients.Semantic proximity Read ↗

Large deletions and splicing-site mutations in the STK11 gene in Peutz-Jeghers Chilean families.Semantic proximity Read ↗

High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.Semantic proximity Read ↗

Two cases of somatic STK11 mosaicism in Danish patients with Peutz-Jeghers syndrome.Semantic proximity Read ↗

Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndrome.Semantic proximity Read ↗

Analysis of STK11 gene variant in five Chinese patients with Peutz-Jeghers syndrome.Semantic proximity Read ↗

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