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First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome.
McKay, Victoria; Cairns, Diane; Gokhale, David; Mountford, Roger; Greenhalgh, Lynn.
Affiliation
  • McKay V; Department of Clinical Genetics, Merseyside and Cheshire Regional Clinical Genetics Service, Liverpool Women's NHS Foundation Trust, Crown Street, Liverpool, L8 7SS, UK. Victoria.mckay@lwh.nhs.uk.
  • Cairns D; Merseyside and Cheshire Regional Molecular Genetics Laboratory, Liverpool Women's NHS Foundation Trust, Crown Street, Liverpool, L8 7SS, UK.
  • Gokhale D; Merseyside and Cheshire Regional Molecular Genetics Laboratory, Liverpool Women's NHS Foundation Trust, Crown Street, Liverpool, L8 7SS, UK.
  • Mountford R; Merseyside and Cheshire Regional Molecular Genetics Laboratory, Liverpool Women's NHS Foundation Trust, Crown Street, Liverpool, L8 7SS, UK.
  • Greenhalgh L; Department of Clinical Genetics, Merseyside and Cheshire Regional Clinical Genetics Service, Liverpool Women's NHS Foundation Trust, Crown Street, Liverpool, L8 7SS, UK.
Fam Cancer ; 15(1): 57-61, 2016 Jan.
Article in En | MEDLINE | ID: mdl-26386697
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Full text: 1 Database: MEDLINE Main subject: Peutz-Jeghers Syndrome / Protein Serine-Threonine Kinases Limits: Female / Humans / Male Language: En Journal: Fam Cancer Journal subject: NEOPLASIAS Year: 2016 Type: Article Affiliation country: United kingdom
Fulltext
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Full text: 1 Database: MEDLINE Main subject: Peutz-Jeghers Syndrome / Protein Serine-Threonine Kinases Limits: Female / Humans / Male Language: En Journal: Fam Cancer Journal subject: NEOPLASIAS Year: 2016 Type: Article Affiliation country: United kingdom