TY  - GEN
AU  - Hennekam,Raoul C M
TI  - Hutchinson-Gilford progeria syndrome: review of the phenotype
SN  - 1552-4825
PY  - 2007///0220
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Cardiovascular Diseases
KW  - pathology
KW  - Child
KW  - Female
KW  - Humans
KW  - Infant
KW  - Lamin Type A
KW  - genetics
KW  - Male
KW  - Models, Genetic
KW  - Mutation
KW  - Osteolysis
KW  - Phenotype
KW  - Progeria
N1  - Publication Type: Journal Article; Review
UR  - https://doi.org/10.1002/ajmg.a.31346
ER  -