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6. [DOMINANT HEREDITARY SYNDROME, COMBINING CRANIO-FACIAL DYSOSTOSIS PECULIAR TYPE, GROWTH INSUFFICIENCY OF CHONDRODYSTROPHIC APPEARANCE, AND MASSIVE THICKENING OF OF THE CORTICES OF LONG BONES]. STANESCO V; MAXIMILIAN C; POENARU S; FLOREA I; STANESCO R; IONESCO V; IOANITIU D Rev Fr Endocrinol Clin; 1963; 4():219-31. PubMed ID: 14049206 [No Abstract] [Full Text] [Related]
7. "Whistling face" deformity in compound cranio-facio-corporal syndrome. Sharma RN; Tandon SN Br Med J; 1970 Oct; 4(5726):33. PubMed ID: 5470434 [No Abstract] [Full Text] [Related]
8. [THE POTTER SYNDROME (BILATERAL RENAL AGENESIS, FACIAL CHANGES AND OLIGOHYDRAMNIOS). STUDY OF A CASE]. RASORE-QUARTINO A; DEPAULINI GC Pathologica; 1963; 55():459-62. PubMed ID: 14153633 [No Abstract] [Full Text] [Related]
9. [ON SOME CASES OF CRANIOFACIAL MALFORMATIONS IN ASSOCIATION WITH OTHER SENSORY ALTERATIONS]. APOLLONIO A; ZOLDAN T Boll Ocul; 1964 Jan; 43():76-84. PubMed ID: 14216075 [No Abstract] [Full Text] [Related]
10. The whistling face syndrome--cranio-carpo-tarsal dysplasia. Report of a case and a survey of the literature. MacLeod P; Patriquin H Clin Pediatr (Phila); 1974 Feb; 13(2):184-9. PubMed ID: 4810704 [No Abstract] [Full Text] [Related]
11. Familial occurrence of the Freeman-Sheldon syndrome: cranio-carpotarsal dysplasia. Gross-Kieselstein E; Abrahamov A; Ben-Hur N Pediatrics; 1971 Jun; 47(6):1064-7. PubMed ID: 5141750 [No Abstract] [Full Text] [Related]
12. [REPORT OF A SPORADIC CLINICAL CASE OF CRANIOFACIAL DYSOSTOSIS OR CROUZON'S DISEASE]. FANTA E; AVENDANO A Pediatria (Santiago); 1963; 6():190-4. PubMed ID: 14080019 [No Abstract] [Full Text] [Related]