125 related articles for article (PubMed ID: 12029347)
21. [Doughnut lesions of the cranial vault: an hereditary bone dysplasia].
Aubé L; Vallières M; Lemay M
Can Assoc Radiol J; 1988 Sep; 39(3):204-8. PubMed ID: 2971055
[TBL] [Abstract][Full Text] [Related]
22. New autosomal recessive syndrome of sparse hair, osteopenia, and mental retardation in Mennonite sisters.
Kaler SG; Garrity AM; Stern HJ; Rosenbaum KN; Orrison BM; Marini JC; Bernardini I; Saal HM
Am J Med Genet; 1992 Aug; 43(6):983-8. PubMed ID: 1415349
[TBL] [Abstract][Full Text] [Related]
23. Short rib-polydactyly syndrome, Majewski type.
Chen H; Yang SS; Gonzalez E; Fowler M; Al Saadi A
Am J Med Genet; 1980; 7(2):215-22. PubMed ID: 7468649
[TBL] [Abstract][Full Text] [Related]
24. Congenital bowing of long bones: clinical and experimental study.
Nogami H; Oohira A; Kuroyanagi M; Mizutani A
Teratology; 1986 Feb; 33(1):1-7. PubMed ID: 3738801
[TBL] [Abstract][Full Text] [Related]
25. Brachyolmia: radiographic and genetic evidence of heterogeneity.
Shohat M; Lachman R; Gruber HE; Rimoin DL
Am J Med Genet; 1989 Jun; 33(2):209-19. PubMed ID: 2669482
[TBL] [Abstract][Full Text] [Related]
26. An autosomal recessive bone dysplasia syndrome resembling hypochondroplasia.
Desch LW; Horton WA
Pediatrics; 1985 Apr; 75(4):786-9. PubMed ID: 4039054
[No Abstract] [Full Text] [Related]
27. New form of bone dysplasia with multiple fractures associated with monosomy X.
Azouz EM; Chen MF; Khalifé S; Cartier L; Eydoux P
Am J Med Genet; 1996 Dec; 66(2):163-8. PubMed ID: 8958323
[TBL] [Abstract][Full Text] [Related]
28. Beyond osteogenesis imperfecta: Causes of fractures during infancy and childhood.
Bronicki LM; Stevenson RE; Spranger JW
Am J Med Genet C Semin Med Genet; 2015 Dec; 169(4):314-27. PubMed ID: 26531771
[TBL] [Abstract][Full Text] [Related]
29. Recessive spondylocostal dysostosis: two new cases.
Silengo MC; Cavallaro S; Franceschini P
Clin Genet; 1978 Mar; 13(3):289-94. PubMed ID: 416928
[TBL] [Abstract][Full Text] [Related]
30. Acromesomelic dysplasia.
Langer LO; Garrett RT
Radiology; 1980 Nov; 137(2):349-55. PubMed ID: 7433666
[TBL] [Abstract][Full Text] [Related]
31. Spondylometaphyseal dysplasia.
Thomas PS; Nevin NC
AJR Am J Roentgenol; 1977 Jan; 128(1):89-93. PubMed ID: 401596
[TBL] [Abstract][Full Text] [Related]
32. Developmental coxa vara associated with spondylometaphyseal dysplasia (DCV/SMD): "SMD-corner fracture type" (DCV/SMD-CF) demonstrated in most reported cases.
Currarino G; Birch JG; Herring JA
Pediatr Radiol; 2000 Jan; 30(1):14-24. PubMed ID: 10663502
[TBL] [Abstract][Full Text] [Related]
33. Spondylocostal dysostosis in South African sisters.
Beighton P; Horan FT
Clin Genet; 1981 Jan; 19(1):23-5. PubMed ID: 7460377
[TBL] [Abstract][Full Text] [Related]
34. Exclusion of the dymeclin and PAPSS2 genes in a novel form of spondyloepimetaphyseal dysplasia and mental retardation.
Geneviève D; Héron D; El Ghouzzi V; Prost-Squarcioni C; Le Merrer M; Jacquette A; Sanlaville D; Pinton F; Villeneuve N; Kalifa G; Munnich A; Cormier-Daire V
Eur J Hum Genet; 2005 May; 13(5):541-6. PubMed ID: 15726110
[TBL] [Abstract][Full Text] [Related]
35. Wedge-shaped epiphyses of the knees in two siblings: a new recessive rare dysplasia?
Bellini F; Chiumello G; Rimoldi R; Weber G
Helv Paediatr Acta; 1984 Oct; 39(4):365-72. PubMed ID: 6543849
[TBL] [Abstract][Full Text] [Related]
36. [Radiologic changes in metaphyseal chondrodystrophy of the McKusick type (cartilage-hair hypoplasia)].
Lischka A; Frisch H; Weissenbacher G
Monatsschr Kinderheilkd; 1984 Jul; 132(7):550-3. PubMed ID: 6472301
[TBL] [Abstract][Full Text] [Related]
37. Spinal involvement in Pyle's disease.
Turra S; Gigante C; Pavanini G; Bardi C
Pediatr Radiol; 2000 Jan; 30(1):25-7. PubMed ID: 10663503
[TBL] [Abstract][Full Text] [Related]
38. A familial syndrome of diaphyseal cortical thickening of the long bones, bowed legs, tendency to fracture and icthyosis.
Koller ME; Maurseth K; Haneberg B; Aarskog D
Pediatr Radiol; 1979 Jul; 8(3):179-82. PubMed ID: 471563
[TBL] [Abstract][Full Text] [Related]
39. [Generalized bone dysplasia].
Hansen HG
Radiologe; 1971 Aug; 11(8):285-8. PubMed ID: 5098940
[No Abstract] [Full Text] [Related]
40. Skeletal dysplasia in perinatal lethal osteogenesis imperfecta. A complex disorder of endochondral and intramembranous ossification.
Marion MJ; Gannon FH; Fallon MD; Mennuti MT; Lodato RF; Kaplan FS
Clin Orthop Relat Res; 1993 Aug; (293):327-37. PubMed ID: 8339500
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]