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Article

Gene symbol: STK11. Disease: Peutz-Jeghers Syndrome.

Human genetics - 1 Oct 2008

Scott Rodney, Crooks Renee, Meldrum Cliff

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Source

Identifiers

PMID: 18846624

Genes

STK11

Provenance

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Related research

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Gene symbol: STK11. Disease: Peutz-Jeghers Syndrome.PMID 18846624Read ↗

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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 ↗

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

Progress report: Peutz-Jeghers syndrome.Semantic proximity Read ↗

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Disease pattern in Danish patients with Peutz-Jeghers syndrome.Semantic proximity Read ↗

Clinical and Molecular Analysis in Patients with Peutz-Jeghers Syndrome.Semantic proximity Read ↗

An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review.Semantic proximity Read ↗

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

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