TY  - GEN
AU  - Laron,Z
TI  - Laron-type dwarfism (hereditary somatomedin deficiency): a review
SN  - 0071-111X
PY  - 1984///0224
KW  - Abnormalities, Multiple
KW  - complications
KW  - Adolescent
KW  - Adult
KW  - Anthropometry
KW  - Blood Glucose
KW  - analysis
KW  - Child
KW  - Child, Preschool
KW  - Dwarfism, Pituitary
KW  - genetics
KW  - Electroencephalography
KW  - Female
KW  - Growth Hormone
KW  - blood
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Pedigree
KW  - Psychological Tests
KW  - Receptors, Cell Surface
KW  - Receptors, Somatotropin
KW  - Sexual Maturation
KW  - Somatomedins
KW  - deficiency
KW  - Syndrome
KW  - Tooth Abnormalities
N1  - Publication Type: Journal Article; Review
UR  - https://doi.org/10.1007/978-3-642-69070-9_3
ER  -