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Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
158 related items for PubMed ID: 3728563
1. Acromicric dysplasia. Maroteaux P, Stanescu R, Stanescu V, Rappaport R. Am J Med Genet; 1986 Jul; 24(3):447-59. PubMed ID: 3728563 [Abstract] [Full Text] [Related]
2. Acromicric dysplasia and geleophysic dysplasia: similarities and differences. Hennekam RC, van Bever Y, Oorthuys JW. Eur J Pediatr; 1996 Apr; 155(4):311-4. PubMed ID: 8777926 [Abstract] [Full Text] [Related]
3. An unknown spondylo-meta-epiphyseal dysplasia in sibs with extreme short stature. Menger H, Mundlos S, Becker K, Spranger J, Zabel B. Am J Med Genet; 1996 May 03; 63(1):80-3. PubMed ID: 8723091 [Abstract] [Full Text] [Related]
4. Lethal short-limbed chondrodysplasia in early infancy. Yang SS, Heidelberger KP, Brough AJ, Corbett DP, Bernstein J. Perspect Pediatr Pathol; 1976 May 03; 3():1-40. PubMed ID: 972830 [Abstract] [Full Text] [Related]
5. Hydrops-ectopic calcification-moth-eaten skeletal dysplasia (Greenberg dysplasia): prenatal diagnosis and further delineation of a rare genetic disorder. Chitayat D, Gruber H, Mullen BJ, Pauzner D, Costa T, Lachman R, Rimoin DL. Am J Med Genet; 1993 Aug 15; 47(2):272-7. PubMed ID: 8213919 [Abstract] [Full Text] [Related]
7. Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritance. Faivre L, Le Merrer M, Baumann C, Polak M, Chatelain P, Sulmont V, Cousin J, Bost M, Cordier MP, Zackai E, Russell K, Finidori G, Pouliquen JC, Munnich A, Maroteaux P, Cormier-Daire V. J Med Genet; 2001 Nov 15; 38(11):745-9. PubMed ID: 11694546 [Abstract] [Full Text] [Related]
8. Kniest dysplasia: radiologic, histopathological, and scanning electronmicroscopic findings. Gilbert-Barnes E, Langer LO, Opitz JM, Laxova R, Sotelo-Arila C. Am J Med Genet; 1996 May 03; 63(1):34-45. PubMed ID: 8723084 [Abstract] [Full Text] [Related]
9. Pathogenic mechanisms in osteochondrodysplasias. Stanescu V, Stanescu R, Maroteaux P. J Bone Joint Surg Am; 1984 Jul 03; 66(6):817-36. PubMed ID: 6376516 [Abstract] [Full Text] [Related]
11. Omodysplasia: an affected mother and son. Venditti CP, Farmer J, Russell KL, Friedrich CA, Alter C, Canning D, Whitaker L, Mennuti MT, Driscoll DA, Zackai EH. Am J Med Genet; 2002 Aug 01; 111(2):169-77. PubMed ID: 12210345 [Abstract] [Full Text] [Related]
13. Geleophysic dysplasia--acromicric dysplasia with evidence of glycoprotein storage. Lipson AH, Kan AE, Kozlowski K. Am J Med Genet Suppl; 1987 Aug 01; 3():181-9. PubMed ID: 3130853 [Abstract] [Full Text] [Related]
14. Desbuquois dysplasia, a reevaluation with abnormal and "normal" hands: radiographic manifestations. Faivre L, Cormier-Daire V, Eliott AM, Field F, Munnich A, Maroteaux P, Le Merrer M, Lachman R. Am J Med Genet A; 2004 Jan 01; 124A(1):48-53. PubMed ID: 14679586 [Abstract] [Full Text] [Related]
15. Fibrochondrogenesis: radiologic and histologic studies. Eteson DJ, Adomian GE, Ornoy A, Koide T, Sugiura Y, Calabro A, Lungarotti S, Mastroiacovo P, Lachman RS, Rimoin DL. Am J Med Genet; 1984 Oct 01; 19(2):277-90. PubMed ID: 6507479 [Abstract] [Full Text] [Related]
16. Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology. Borochowitz Z, Langer LO, Gruber HE, Lachman R, Katznelson MB, Rimoin DL. Am J Med Genet; 1993 Feb 01; 45(3):320-6. PubMed ID: 8434618 [Abstract] [Full Text] [Related]
17. Familial recurrence of geleophysic dysplasia. Koiffmann CP, Wajntal A, Ursich MJ, Pupo AA. Am J Med Genet; 1984 Nov 01; 19(3):483-6. PubMed ID: 6507494 [Abstract] [Full Text] [Related]
18. New X linked spondyloepimetaphyseal dysplasia: report on eight affected males in the same family. Camera G, Stella G, Camera A. J Med Genet; 1994 May 01; 31(5):371-6. PubMed ID: 8064814 [Abstract] [Full Text] [Related]
19. [The "Fantasy Island" syndrome. Identification of a new osteochondrodysplasia probably of autosomal dominant type]. Cantú JM. Gac Med Mex; 1995 May 01; 131(1):23-6; discussion 27. PubMed ID: 7493737 [Abstract] [Full Text] [Related]