Descriptor
| Heredity | 7 |
| Exceptional Child Research | 6 |
| Special Health Problems | 5 |
| Medical Evaluation | 4 |
| Medical Case Histories | 3 |
| Congenital Impairments | 2 |
| Dietetics | 2 |
| Genetics | 2 |
| Medical Research | 2 |
| Metabolism | 2 |
| Pathology | 2 |
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Source
| Pediatrics | 7 |
Author
| Danks, David M. | 1 |
| Dees, Susan Coons | 1 |
| Fishler, K. | 1 |
| Hsia, Y. E. | 1 |
| Scheikholislam, Bagher M. | 1 |
| Schneck, Larry | 1 |
| Stemfel, Robert S., Jr. | 1 |
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Peer reviewedDees, Susan Coons – Pediatrics, 1972
Descriptors: Allergy, Clinical Diagnosis, Dietetics, Exceptional Child Research
Peer reviewedHsia, Y. E.; And Others – Pediatrics, 1971
Reported are seven cases in two families of the Meckel syndrome, whose key features are occipital encephalocele, cleft lip and palate, polydactyly, and polycystic kidneys. Evidence supports the hypothesis that the syndrome is a recessively inherited condition, determined by homozygous expression of a single autosomal gene. (Author/KW)
Descriptors: Congenital Impairments, Exceptional Child Research, Genetics, Heredity
Peer reviewedPediatrics, 1976
Descriptors: Congenital Impairments, Counseling, Definitions, Exceptional Child Services
Peer reviewedSchneck, Larry; And Others – Pediatrics, 1972
Descriptors: Exceptional Child Research, Heredity, Jews, Medical Evaluation
Peer reviewedFishler, K.; And Others – Pediatrics, 1972
Descriptors: Dietetics, Diseases, Exceptional Child Research, Heredity
Peer reviewedScheikholislam, Bagher M.; Stemfel, Robert S., Jr. – Pediatrics, 1972
The clinical and laboratory appraisal of a familial isolated growth hormone deficiency is reported. (Author)
Descriptors: Exceptional Child Research, Growth Patterns, Heredity, Medical Case Histories
Peer reviewedDanks, David M.; And Others – Pediatrics, 1972
Descriptors: Etiology, Exceptional Child Research, Heredity, Medical Case Histories
