TY  - GEN
AU  - Isik,Esra
AU  - Simsir,Ozguc Semih
AU  - Solmaz,Asli Ece
AU  - Onay,Huseyin
AU  - Atik,Tahir
AU  - Aykut,Ayca
AU  - Durmaz,Asude
AU  - Cogulu,Ozgur
AU  - Ozkinay,Ferda
TI  - Clinical and molecular aspects of PTEN mutations in 10 pediatric patients
SN  - 1469-1809
PY  - 2021///0322
KW  - Adolescent
KW  - Child
KW  - Child, Preschool
KW  - Exons
KW  - Female
KW  - Genotype
KW  - Hamartoma Syndrome, Multiple
KW  - diagnosis
KW  - Humans
KW  - Infant
KW  - Male
KW  - Mutation
KW  - PTEN Phosphohydrolase
KW  - genetics
KW  - Pedigree
KW  - Phenotype
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1111/ahg.12380
ER  -