Descriptor
| Exceptional Child Research | 2 |
| Genetics | 2 |
| Medical Research | 2 |
| Mental Retardation | 2 |
| Biochemistry | 1 |
| Congenital Impairments | 1 |
| Identification | 1 |
| Incidence | 1 |
| Medical Evaluation | 1 |
| Severe Disabilities | 1 |
Source
| Journal of Pediatrics | 2 |
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Peer reviewedGriffin, Robert F.; Elsas, Louis J. – Journal of Pediatrics, 1975
In an attempt to improve the identification of the asymptomatic carrier of classic phenylketonuria (PKU) 59 male and female normal control Ss were differentiated from 18 males and females heterozgous for PKU. (DB)
Descriptors: Biochemistry, Exceptional Child Research, Genetics, Identification
Peer reviewedDanks, David M.; And Others – Journal of Pediatrics, 1975
Examined were eight patients with cerebro-hepato-renal syndrome of Zellweger (associated with severe cerebral dysfunction, hypotonia and unusual appearance). (CL)
Descriptors: Congenital Impairments, Exceptional Child Research, Genetics, Incidence
