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Tong H, Zhang X, Meng X, Lu L, Mai D, Qu S
Guo M, et al
1B and Tables 57)
Additional conditions under the umbrella of congenital IGF-1 deficiencies include a documented case of a 15-year-old boy suffering from severe prenatal and postnatal growth failure, sensorineural deafness and mental retardation due to a homozygous partial deletion of the IGF-I gene [41] as well as IGF1R genes defects [42]
