PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability.
|
28475857 |
2017 |
Hamartoma Syndrome, Multiple
|
|
0.700 |
GeneticVariation
|
CLINVAR |
KLLN epigenotype-phenotype associations in Cowden syndrome.
|
25669429 |
2015 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
KLLN epigenotype-phenotype associations in Cowden syndrome.
|
25669429 |
2015 |
Hamartoma Syndrome, Multiple
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Second malignant neoplasms in patients with Cowden syndrome with underlying germline PTEN mutations.
|
24778394 |
2014 |
Brain Neoplasms
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Combined PTEN Mutation and Protein Expression Associate with Overall and Disease-Free Survival of Glioblastoma Patients.
|
24721394 |
2014 |
Brain Neoplasms
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Prospective enterprise-level molecular genotyping of a cohort of cancer patients.
|
25157968 |
2014 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
GeneticVariation
|
CLINVAR |
PIK3CA and PTEN gene and exon mutation-specific clinicopathologic and molecular associations in colorectal cancer.
|
23633456 |
2013 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
GeneticVariation
|
CLINVAR |
High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome.
|
23335809 |
2013 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome.
|
23335809 |
2013 |
Hamartoma Syndrome, Multiple
|
|
0.700 |
GeneticVariation
|
CLINVAR |
PTEN hamartoma tumor syndrome and Gorham-Stout phenomenon.
|
22628360 |
2012 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
GeneticVariation
|
CLINVAR |
A comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromes.
|
21828076 |
2011 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.
|
20533527 |
2010 |
Hamartoma Syndrome, Multiple
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Lhermitte-Duclos disease caused by a novel germline PTEN mutation R173P in a patient presenting with psychosis.
|
19719509 |
2010 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Lhermitte-Duclos disease caused by a novel germline PTEN mutation R173P in a patient presenting with psychosis.
|
19719509 |
2010 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.
|
20533527 |
2010 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.
|
19265751 |
2009 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
GeneticVariation
|
CLINVAR |
The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.
|
19265751 |
2009 |
Hamartoma Syndrome, Multiple
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers.
|
17526800 |
2007 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers.
|
17526800 |
2007 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers.
|
17526800 |
2007 |
Hamartoma Syndrome, Multiple
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Functional evaluation of PTEN missense mutations using in vitro phosphoinositide phosphatase assay.
|
10866302 |
2000 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
CausalMutation
|
CLINVAR |
Functional evaluation of PTEN missense mutations using in vitro phosphoinositide phosphatase assay.
|
10866302 |
2000 |
Neoplastic Syndromes, Hereditary
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Functional evaluation of PTEN missense mutations using in vitro phosphoinositide phosphatase assay.
|
10866302 |
2000 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
GeneticVariation
|
CLINVAR |
Functional evaluation of PTEN missense mutations using in vitro phosphoinositide phosphatase assay.
|
10866302 |
2000 |
PTEN Hamartoma Tumor Syndrome
|
|
0.700 |
GeneticVariation
|
CLINVAR |
PTEN mutations in gliomas and glioneuronal tumors.
|
9619835 |
1998 |