The spectrum and evolution of phenotypic finding... [J Med Genet. 2001] - PubMed

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PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. [Hum Mol Genet. 1999]
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.
Marsh DJ, Kum JB, Lunetta KL, Bennett MJ, Gorlin RJ, Ahmed SF, Bodurtha J, Crowe C, Curtis MA, Dasouki M, et al. Hum Mol Genet. 1999 Aug; 8(8):1461-72.
Germline PTEN mutation in a family with Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome. [Am J Med Genet. 1998]
Germline PTEN mutation in a family with Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome.
Zori RT, Marsh DJ, Graham GE, Marliss EB, Eng C. Am J Med Genet. 1998 Dec 4; 80(4):399-402.
Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN. [J Med Genet. 1999]
Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN.
Celebi JT, Tsou HC, Chen FF, Zhang H, Ping XL, Lebwohl MG, Kezis J, Peacocke M. J Med Genet. 1999 May; 36(5):360-4.
Review Mutations of the human PTEN gene. [Hum Mutat. 2000]
Review Mutations of the human PTEN gene.
Bonneau D, Longy M. Hum Mutat. 2000; 16(2):109-22.
Review PTEN: one gene, many syndromes. [Hum Mutat. 2003]
Review PTEN: one gene, many syndromes.
Eng C. Hum Mutat. 2003 Sep; 22(3):183-98.

Familial follicular cell-derived thyroid carcinoma. [Front Endocrinol (Lausanne). 2...]
Familial follicular cell-derived thyroid carcinoma.
Son EJ, Nosé V. Front Endocrinol (Lausanne). 2012; 3:61. Epub 2012 May 3.
Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations. [J Clin Endocrinol Metab. 2011]
Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations.
Ngeow J, Mester J, Rybicki LA, Ni Y, Milas M, Eng C. J Clin Endocrinol Metab. 2011 Dec; 96(12):E2063-71. Epub 2011 Sep 28.
A mutant form of PTEN linked to autism. [Protein Sci. 2010]
A mutant form of PTEN linked to autism.
Redfern RE, Daou MC, Li L, Munson M, Gericke A, Ross AH. Protein Sci. 2010 Oct; 19(10):1948-56.

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The spectrum and evolution of phenotypic findings in PTEN mutation positive case...
The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome.
J Med Genet. 2001 Jan ;38(1):52-8.

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