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2. [C brachydactyly in four generations]. Aksu F; Mietens C Klin Padiatr; 1984; 196(1):52-4. PubMed ID: 6694344 [TBL] [Abstract][Full Text] [Related]
3. Familial brachydactyly and chondrocalcinosis. Report of a patient, pedigree and review of the literature. Mathews JL; Samuelson CO; Manis S J Rheumatol; 1983 Oct; 10(5):819-22. PubMed ID: 6644710 [TBL] [Abstract][Full Text] [Related]
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7. The trichorhinophalangeal syndrome. Report of 4 familial cases belonging to 4 generations. Ferrández A; Remírez J; Sáenz P; Calvo M Helv Paediatr Acta; 1980 Dec; 35(6):559-67. PubMed ID: 7204100 [TBL] [Abstract][Full Text] [Related]
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9. Hereditary multiple exostoses. Report of a family. Crandall BF; Field LL; Sparkes RS; Spence MA Clin Orthop Relat Res; 1984 Nov; (190):217-9. PubMed ID: 6333306 [TBL] [Abstract][Full Text] [Related]
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11. The "long-thumb" brachydactyly syndrome. Hollister DW; Hollister WG Am J Med Genet; 1981; 8(1):5-16. PubMed ID: 7246605 [TBL] [Abstract][Full Text] [Related]
12. Corneal changes, hyperkeratosis, short stature, brachydactyly, and premature birth: a new autosomal dominant syndrome. Stern JK; Lubinsky MS; Durrie DS; Luckasen JR Am J Med Genet; 1984 May; 18(1):67-77. PubMed ID: 6234802 [TBL] [Abstract][Full Text] [Related]
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14. Ruvalcaba syndrome: autosomal dominant inheritance. Sugio Y; Kajii T Am J Med Genet; 1984 Dec; 19(4):741-53. PubMed ID: 6517098 [TBL] [Abstract][Full Text] [Related]
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18. Six generations of a family with multiple limb deficiencies. Helal A; Perry T; Ogden JA; Greene TL J Pediatr Orthop; 1993; 13(2):210-3. PubMed ID: 8459013 [TBL] [Abstract][Full Text] [Related]
19. Family study of the inheritance of pectus excavatum. Creswick HA; Stacey MW; Kelly RE; Gustin T; Nuss D; Harvey H; Goretsky MJ; Vasser E; Welch JC; Mitchell K; Proud VK J Pediatr Surg; 2006 Oct; 41(10):1699-703. PubMed ID: 17011272 [TBL] [Abstract][Full Text] [Related]
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