TY  - GEN
AU  - Linden,Helen C
AU  - Price,Susan M
TI  - Cardiofaciocutaneous syndrome in a mother and two sons with a MEK2 mutation
SN  - 1473-5717
PY  - 2011///0627
KW  - Adult
KW  - Adult Children
KW  - Aged
KW  - Ectodermal Dysplasia
KW  - diagnosis
KW  - Facies
KW  - Failure to Thrive
KW  - Female
KW  - Heart Defects, Congenital
KW  - Heredity
KW  - Humans
KW  - Keratoderma, Palmoplantar
KW  - Lentigo
KW  - congenital
KW  - MAP Kinase Kinase 2
KW  - genetics
KW  - Male
KW  - Middle Aged
KW  - Mothers
KW  - Mutation, Missense
KW  - Myopia
KW  - Pedigree
KW  - Polyhydramnios
KW  - Pregnancy
KW  - Pulmonary Valve Stenosis
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1097/MCD.0b013e32833ff29d
ER  -