000 01340 a2200457 4500
005 20250518091540.0
264 0 _c20210322
008 202103s 0 0 eng d
022 _a1469-1809
024 7 _a10.1111/ahg.12380
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aIsik, Esra
245 0 0 _aClinical and molecular aspects of PTEN mutations in 10 pediatric patients.
_h[electronic resource]
260 _bAnnals of human genetics
_c07 2020
300 _a324-330 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aExons
650 0 4 _aFemale
650 0 4 _aGenotype
650 0 4 _aHamartoma Syndrome, Multiple
_xdiagnosis
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPTEN Phosphohydrolase
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPhenotype
700 1 _aSimsir, Ozguc Semih
700 1 _aSolmaz, Asli Ece
700 1 _aOnay, Huseyin
700 1 _aAtik, Tahir
700 1 _aAykut, Ayca
700 1 _aDurmaz, Asude
700 1 _aCogulu, Ozgur
700 1 _aOzkinay, Ferda
773 0 _tAnnals of human genetics
_gvol. 84
_gno. 4
_gp. 324-330
856 4 0 _uhttps://doi.org/10.1111/ahg.12380
_zAvailable from publisher's website
999 _c30733070
_d30733070