-
1
-
-
0027477670
-
The histopathology of fibrodysplasia ossificans progressiva. An endochondral process
-
Kaplan FS, Tabas JA, Gannon FH, Finkel G, Hahn GV, Zasloff MA (1993) The histopathology of fibrodysplasia ossificans progressiva. An endochondral process. J Bone Joint Surg (Am) 75:220-230.
-
(1993)
J Bone Joint Surg (Am)
, vol.75
, pp. 220-230
-
-
Kaplan, F.S.1
Tabas, J.A.2
Gannon, F.H.3
Finkel, G.4
Hahn, G.V.5
Zasloff, M.A.6
-
2
-
-
25844487690
-
The phenotype of fibrodysplasia ossificans progressiva
-
Kaplan FS, Glaser DL, Shore EM, Deirmengian GK, Gupta R, Delai P, Morhart R, Smith R, Le Merrer M, Rogers JG, Connor JM, Kitterman JA (2005a) The phenotype of fibrodysplasia ossificans progressiva. Clin Rev Bone Min Metab 3:183-188.
-
(2005)
Clin Rev Bone Min Metab
, vol.3
, pp. 183-188
-
-
Kaplan, F.S.1
Glaser, D.L.2
Shore, E.M.3
Deirmengian, G.K.4
Gupta, R.5
Delai, P.6
Morhart, R.7
Smith, R.8
Le Merrer, M.9
Rogers, J.G.10
Connor, J.M.11
Kitterman, J.A.12
-
3
-
-
0027403045
-
The natural history of heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. A study of forty-four patients
-
Cohen RB, Hahn GV, Tabas JA, Peeper J, Levitz CL, Sando A, Sando N, Zasloff M, Kaplan FS (1993) The natural history of heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. A study of forty-four patients. J Bone Joint Surg (Am) 75:215-219.
-
(1993)
J Bone Joint Surg (Am)
, vol.75
, pp. 215-219
-
-
Cohen, R.B.1
Hahn, G.V.2
Tabas, J.A.3
Peeper, J.4
Levitz, C.L.5
Sando, A.6
Sando, N.7
Zasloff, M.8
Kaplan, F.S.9
-
4
-
-
0028287031
-
Ageand joint-specific risk of initial heterotopic ossification in patients who have fibrodysplasia ossificans progressiva
-
Rocke DM, Zasloff M, Peeper J, Cohen RB, Kaplan FS (1994) Ageand joint-specific risk of initial heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. Clin Orthop 301:243-248.
-
(1994)
Clin Orthop
, vol.301
, pp. 243-248
-
-
Rocke, D.M.1
Zasloff, M.2
Peeper, J.3
Cohen, R.B.4
Kaplan, F.S.5
-
5
-
-
0031059563
-
Bone morphogenetic protein (BMP) 2/4 in early fibromatous lesions of fibrodysplasia ossificans progressiva
-
Gannon FH, Kaplan FS, Olmsted E, Finkel GC, Zasloff M, Shore E (1997) Bone morphogenetic protein (BMP) 2/4 in early fibromatous lesions of fibrodysplasia ossificans progressiva. Hum Pathol 28:339-343.
-
(1997)
Hum Pathol
, vol.28
, pp. 339-343
-
-
Gannon, F.H.1
Kaplan, F.S.2
Olmsted, E.3
Finkel, G.C.4
Zasloff, M.5
Shore, E.6
-
6
-
-
0029012733
-
Permanent heterotopic ossification at the injection site after diphtheria-tetanus-pertussis immunizations in children who have fibrodysplasia ossificans progressiva
-
Lanchoney TF, Cohen RB, Rocke DM, Zasloff MA, Kaplan FS (1995) Permanent heterotopic ossification at the injection site after diphtheria-tetanus- pertussis immunizations in children who have fibrodysplasia ossificans progressiva. J Pediatr 126:762-764.
-
(1995)
J Pediatr
, vol.126
, pp. 762-764
-
-
Lanchoney, T.F.1
Cohen, R.B.2
Rocke, D.M.3
Zasloff, M.A.4
Kaplan, F.S.5
-
7
-
-
25844459979
-
Treatment considerations for the management of fibrodysplasia ossificans progressiva
-
Glaser DL, Kaplan FS (2005) Treatment considerations for the management of fibrodysplasia ossificans progressiva. Clin Rev Bone Min Metab 3:243-250.
-
(2005)
Clin Rev Bone Min Metab
, vol.3
, pp. 243-250
-
-
Glaser, D.L.1
Kaplan, F.S.2
-
8
-
-
2942750256
-
Influenza-like viral illnesses and flare-ups of fibrodysplasia ossificans progressiva
-
Scarlett RF, Rocke DM, Kantanie S, Patel JB, Shore EM, Kaplan FS (2004) Influenza-like viral illnesses and flare-ups of fibrodysplasia ossificans progressiva. Clin Orthop 423:275-279.
-
(2004)
Clin Orthop
, vol.423
, pp. 275-279
-
-
Scarlett, R.F.1
Rocke, D.M.2
Kantanie, S.3
Patel, J.B.4
Shore, E.M.5
Kaplan, F.S.6
-
9
-
-
0029043815
-
Mild expression of fibrodysplasia ossificans progressiva: A report of 3 cases
-
Janoff HB, Tabas JA, Shore EM, Muenke M, Dalinka MK, Schlesinger S, Zasloff MA, Kaplan FS (1995) Mild expression of fibrodysplasia ossificans progressiva: A report of 3 cases. J Rheumatol 22:976-978.
-
(1995)
J Rheumatol
, vol.22
, pp. 976-978
-
-
Janoff, H.B.1
Tabas, J.A.2
Shore, E.M.3
Muenke, M.4
Dalinka, M.K.5
Schlesinger, S.6
Zasloff, M.A.7
Kaplan, F.S.8
-
10
-
-
25844469044
-
Immunological features of fibrodysplasia ossificans progressiva and the dysregulated BMP4 pathway
-
Kaplan FS, Shore EM, Gupta R, Billings PC, Glaser DL, Pignolo RJ, Graf D, Kamoun M (2005b) Immunological features of fibrodysplasia ossificans progressiva and the dysregulated BMP4 pathway. Clin Rev Bone Min Metab 3:189-193.
-
(2005)
Clin Rev Bone Min Metab
, vol.3
, pp. 189-193
-
-
Kaplan, F.S.1
Shore, E.M.2
Gupta, R.3
Billings, P.C.4
Glaser, D.L.5
Pignolo, R.J.6
Graf, D.7
Kamoun, M.8
-
11
-
-
0030209816
-
Fibrodysplasia ossificans progressiva: Searching for the skeleton key
-
Kaplan FS, Shore EM, Zasloff MA (1996) Fibrodysplasia ossificans progressiva: searching for the skeleton key. Calcif Tissue Int 59:75-78.
-
(1996)
Calcif Tissue Int
, vol.59
, pp. 75-78
-
-
Kaplan, F.S.1
Shore, E.M.2
Zasloff, M.A.3
-
12
-
-
0031984796
-
Acute lymphocytic infiltration in an extremely early lesion of fibrodysplasia ossificans progressiva
-
Gannon FH, Valentine BA, Shore EM, Zasloff MA, Kaplan FS (1998) Acute lymphocytic infiltration in an extremely early lesion of fibrodysplasia ossificans progressiva. Clin Orthop 346:19-25.
-
(1998)
Clin Orthop
, vol.346
, pp. 19-25
-
-
Gannon, F.H.1
Valentine, B.A.2
Shore, E.M.3
Zasloff, M.A.4
Kaplan, F.S.5
-
14
-
-
0016757780
-
On the origin of cells in heterotopic bone formation
-
Buring K (1975) On the origin of cells in heterotopic bone formation. Clin Orthop 110:293-302.
-
(1975)
Clin Orthop
, vol.110
, pp. 293-302
-
-
Buring, K.1
-
15
-
-
0029746491
-
Overexpression of an osteogenic morphogen in fibrodysplasia ossificans progressiva
-
Shafritz AB, Shore EM, Gannon FH, Zasloff MA, Taub R, Muenke M, Kaplan FS (1996) Overexpression of an osteogenic morphogen in fibrodysplasia ossificans progressiva. N Engl J Med 335:555-561.
-
(1996)
N Engl J Med
, vol.335
, pp. 555-561
-
-
Shafritz, A.B.1
Shore, E.M.2
Gannon, F.H.3
Zasloff, M.A.4
Taub, R.5
Muenke, M.6
Kaplan, F.S.7
-
16
-
-
33744773190
-
Dysregulation of the BMP-4 signaling pathway in fibrodysplasia ossificans progressiva
-
Kaplan FS, Fiori J, L S D L P, Ahn J, Billings PC, Shore EM (2006) Dysregulation of the BMP-4 signaling pathway in fibrodysplasia ossificans progressiva. Ann NY Acad Sci 1068:54-65.
-
(2006)
Ann NY Acad Sci
, vol.1068
, pp. 54-65
-
-
Kaplan, F.S.1
Fiori, J.2
Lo, S.D.L.P.3
Ahn, J.4
Billings, P.C.5
Shore, E.M.6
-
17
-
-
20844450082
-
Fibrodysplasia ossificans progressiva (FOP), a disorder of ectopic osteogenesis, misregulates cell surface expression and trafficking of BMPRIA
-
De La Pena LS, Billings PC, Fiori JL, Ahn J, Kaplan FS, Shore EM (2005) Fibrodysplasia ossificans progressiva (FOP), a disorder of ectopic osteogenesis, misregulates cell surface expression and trafficking of BMPRIA. J Bone Miner Res 20:1168-1176.
-
(2005)
J Bone Miner Res
, vol.20
, pp. 1168-1176
-
-
De La Pena, L.S.1
Billings, P.C.2
Fiori, J.L.3
Ahn, J.4
Kaplan, F.S.5
Shore, E.M.6
-
18
-
-
33646865518
-
Dysregulation of the BMP-p38 MAPK signaling pathway in cells from patients with fibrodysplasia ossificans progressiva (FOP)
-
Fiori JL, Billings PC, Serrano De La Peña L, Kaplan FS, Shore EM (2006) Dysregulation of the BMP-p38 MAPK signaling pathway in cells from patients with fibrodysplasia ossificans progressiva (FOP). J Bone Miner Res 21:902-909.
-
(2006)
J Bone Miner Res
, vol.21
, pp. 902-909
-
-
Fiori, J.L.1
Billings, P.C.2
Serrano De La Peña, L.3
Kaplan, F.S.4
Shore, E.M.5
-
19
-
-
25844491030
-
Fibrodysplasia ossificans progressiva and progressive osseous heteroplasia: Two genetic disorders of heterotopic ossification
-
Shore EM, Kaplan FS (2005) Fibrodysplasia ossificans progressiva and progressive osseous heteroplasia: two genetic disorders of heterotopic ossification. Clin Rev Bone Min Metab 3:257-260.
-
(2005)
Clin Rev Bone Min Metab
, vol.3
, pp. 257-260
-
-
Shore, E.M.1
Kaplan, F.S.2
-
20
-
-
25844516368
-
Three pairs of monozygotic twins with fibrodysplasia ossificans progressiva
-
Hebela N, Shore EM, Kaplan FS (2005) Three pairs of monozygotic twins with fibrodysplasia ossificans progressiva. Clin Rev Bone Min Metab 3:205-208.
-
(2005)
Clin Rev Bone Min Metab
, vol.3
, pp. 205-208
-
-
Hebela, N.1
Shore, E.M.2
Kaplan, F.S.3
-
21
-
-
0028348430
-
Progressive osseous heteroplasia: A distinct developmental disorder of heterotopic ossification. Two new case reports and follow-up of three previously reported cases
-
Kaplan FS, Craver R, MacEwen GD, Gannon FH, Finkel G, Hahn G, Tabas J, Gardner RJ, Zasloff MA (1994) Progressive osseous heteroplasia: a distinct developmental disorder of heterotopic ossification. Two new case reports and follow-up of three previously reported cases. J Bone Joint Surg (Am) 76:425-436.
-
(1994)
J Bone Joint Surg (Am)
, vol.76
, pp. 425-436
-
-
Kaplan, F.S.1
Craver, R.2
MacEwen, G.D.3
Gannon, F.H.4
Finkel, G.5
Hahn, G.6
Tabas, J.7
Gardner, R.J.8
Zasloff, M.A.9
-
22
-
-
0002919409
-
Pseudohypoparathyroidism
-
Bilezikian JP, Raisz LG, Rodan GA eds, Academic Press, New York
-
Levine MA (1996) Pseudohypoparathyroidism. In: Bilezikian JP, Raisz LG, Rodan GA (eds) Principles of Bone Biology. Academic Press, New York, pp 853-876.
-
(1996)
Principles of Bone Biology
, pp. 853-876
-
-
Levine, M.A.1
-
23
-
-
0037050365
-
Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasia
-
Shore EM, Ahn J, Jan De Beur S, Li M, Xu M, Gardner RJ, Zasloff MA, Whyte MP, Levine MA, Kaplan FS (2002) Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasia. N Engl J Med 346:99-106.
-
(2002)
N Engl J Med
, vol.346
, pp. 99-106
-
-
Shore, E.M.1
Ahn, J.2
Jan De Beur, S.3
Li, M.4
Xu, M.5
Gardner, R.J.6
Zasloff, M.A.7
Whyte, M.P.8
Levine, M.A.9
Kaplan, F.S.10
-
25
-
-
0029078683
-
Progressive osseous heteroplasia in male patients. Two new case reports
-
Rosenfeld SR, Kaplan FS (1995) Progressive osseous heteroplasia in male patients. Two new case reports. Clin Orthop 317:243-245.
-
(1995)
Clin Orthop
, vol.317
, pp. 243-245
-
-
Rosenfeld, S.R.1
Kaplan, F.S.2
-
27
-
-
0031667304
-
Progressive osseous heteroplasia. Report of a family
-
Urtizberea JA, Testart H, Cartault F, Boccon-Gibod L, Le Merrer M, Kaplan FS (1998) Progressive osseous heteroplasia. Report of a family. J Bone Joint Surg (Br) 80:768-771.
-
(1998)
J Bone Joint Surg (Br)
, vol.80
, pp. 768-771
-
-
Urtizberea, J.A.1
Testart, H.2
Cartault, F.3
Boccon-Gibod, L.4
Le Merrer, M.5
Kaplan, F.S.6
-
28
-
-
0029103048
-
Progressive osseous heteroplasia, uncommon cause of soft tissue ossification: A case report and review of the literature
-
Rodriguez-Jurado R, Gonzalez-Crussi F, Poznanski AK (1995) Progressive osseous heteroplasia, uncommon cause of soft tissue ossification: a case report and review of the literature. Pediatr Pathol Lab Med 15:813-827.
-
(1995)
Pediatr Pathol Lab Med
, vol.15
, pp. 813-827
-
-
Rodriguez-Jurado, R.1
Gonzalez-Crussi, F.2
Poznanski, A.K.3
-
30
-
-
0017290429
-
Chondro-osseous pathology in the chondrodystrophies
-
Rimoin DL, Silberberg R, Hollister DW (1976) Chondro-osseous pathology in the chondrodystrophies. Clin Orthop 114:137-152.
-
(1976)
Clin Orthop
, vol.114
, pp. 137-152
-
-
Rimoin, D.L.1
Silberberg, R.2
Hollister, D.W.3
-
31
-
-
0028940363
-
De novo 1;10 balanced translocation in an infant with thanatophoric dysplasia: A clue to the locus of the candidate gene
-
Hersh, JH, Yen FF, Peiper SC, Barch MJ, Yacoub OA, Voss DH, Roberts JL (1995) De novo 1;10 balanced translocation in an infant with thanatophoric dysplasia: a clue to the locus of the candidate gene. J Med Genet 32:293-295.
-
(1995)
J Med Genet
, vol.32
, pp. 293-295
-
-
Hersh, J.H.1
Yen, F.F.2
Peiper, S.C.3
Barch, M.J.4
Yacoub, O.A.5
Voss, D.H.6
Roberts, J.L.7
-
32
-
-
0028945785
-
A radiographic, morphologic, biochemical and molecular analysis of a case of achondrogenesis type II resulting from substitution for a glycine residue (Gly691-to-Arg) in the type II collagen trimer
-
Mortier GR, Wilkin DJ, Wilcox, et al. (1995) A radiographic, morphologic, biochemical and molecular analysis of a case of achondrogenesis type II resulting from substitution for a glycine residue (Gly691-to-Arg) in the type II collagen trimer. Hum Molec Genet 4:285-288.
-
(1995)
Hum Molec Genet
, vol.4
, pp. 285-288
-
-
Mortier, G.R.1
Wilkin, D.J.2
Wilcox3
-
33
-
-
0032548931
-
Structurally abnormal Type II collagen in a severe form of Kniest Dysplasia caused by an exon 24 skipping mutation
-
Feb. 20
-
Weis MA, Wilkin D, Kim H et al., (Feb. 20 1998) Structurally abnormal Type II collagen in a severe form of Kniest Dysplasia caused by an exon 24 skipping mutation. J Biol Chem 273(8):4761-8.
-
(1998)
J Biol Chem
, vol.273
, Issue.8
, pp. 4761-4768
-
-
Weis, M.A.1
Wilkin, D.2
Kim, H.3
-
34
-
-
0028093135
-
Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia
-
Rousseau F, Bonaventure J, Legeai-Mallet L, Pelet A, Rozet J-M, Maroteaux P, Le Merrer M, Munnich A (1994) Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia. Nature 371:252-254.
-
(1994)
Nature
, vol.371
, pp. 252-254
-
-
Rousseau, F.1
Bonaventure, J.2
Legeai-Mallet, L.3
Pelet, A.4
Rozet, J.-M.5
Maroteaux, P.6
Le Merrer, M.7
Munnich, A.8
-
35
-
-
0027964261
-
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
-
Shiang R, Thompson LM, Zhu Y-Z, Church DM, Fielder TJ, Bocian M, Winokur ST, Wasmuth J J (1994) Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia. Cell 78:335-342.
-
(1994)
Cell
, vol.78
, pp. 335-342
-
-
Shiang, R.1
Thompson, L.M.2
Zhu, Y.-Z.3
Church, D.M.4
Fielder, T.J.5
Bocian, M.6
Winokur, S.T.7
Wasmuth, J.J.8
-
36
-
-
33751330697
-
Novel FGFR3 mutations creating cysteine residues in the extracellular domain of the receptor cause achondroplasia or severe forms of hypochondroplasia
-
Heuertz S, Le Merrer M, Zabel B, et al. (2006) Novel FGFR3 mutations creating cysteine residues in the extracellular domain of the receptor cause achondroplasia or severe forms of hypochondroplasia. Europ J Hum Genet 14 1240-1247.
-
(2006)
Europ J Hum Genet
, vol.14
, pp. 1240-1247
-
-
Heuertz, S.1
Le Merrer, M.2
Zabel, B.3
-
37
-
-
33751342936
-
Erratum
-
Note:, only
-
Note: Erratum: Europ. J. Hum. Genet. 14:1321 only, 2006.
-
(2006)
Europ. J. Hum. Genet.
, vol.14
, pp. 1321
-
-
-
38
-
-
0029035708
-
Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia
-
Hecht JT, Nelson LD, Crowder E, et al. (1995) Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia. Nature Genet 10:325-329.
-
(1995)
Nature Genet
, vol.10
, pp. 325-329
-
-
Hecht, J.T.1
Nelson, L.D.2
Crowder, E.3
-
39
-
-
0027475225
-
Multiple epiphyseal dysplasia, Fairbank type: Morphologic and biochemical study of cartilage
-
Stanescu R, Stanescu V, Muriel M-P, Maroteaux P, (1993) Multiple epiphyseal dysplasia, Fairbank type: morphologic and biochemical study of cartilage. Am J Med Genet 45:501-507.
-
(1993)
Am J Med Genet
, vol.45
, pp. 501-507
-
-
Stanescu, R.1
Stanescu, V.2
Muriel, M.-P.3
Maroteaux, P.4
-
40
-
-
0029786774
-
Defective growth hormone secretion in children with pycnodysostosis and improved linear growth after growth hormone treatment
-
Soliman AT, Rajab A, Al Salmi I, Darwish A, Asfour M (1996) Defective growth hormone secretion in children with pycnodysostosis and improved linear growth after growth hormone treatment. Arch Dis Child 75:242-244
-
(1996)
Arch Dis Child
, vol.75
, pp. 242-244
-
-
Soliman, A.T.1
Rajab, A.2
Al Salmi, I.3
Darwish, A.4
Asfour, M.5
-
42
-
-
0033848677
-
Type V osteogenesis imperfecta: A new form of brittle bone disease
-
Sep
-
Glorieux FH, Rauch F, Plotkin H, et al. (Sep. 2000) Type V osteogenesis imperfecta: a new form of brittle bone disease. Bone Miner Res 15(9):1650-8.
-
(2000)
Bone Miner Res
, vol.15
, Issue.9
, pp. 1650-1658
-
-
Glorieux, F.H.1
Rauch, F.2
Plotkin, H.3
-
43
-
-
0036133709
-
Osteogenesis imperfecta type VI: A form of brittle bone disease with a mineralization defect
-
Jan
-
Glorieux FH, Ward LM, Rauch F, et al. (Jan 2002) Osteogenesis imperfecta type VI: a form of brittle bone disease with a mineralization defect. J Bone Miner Res 17(1):3-8.
-
(2002)
J Bone Miner Res
, vol.17
, Issue.1
, pp. 3-8
-
-
Glorieux, F.H.1
Ward, L.M.2
Rauch, F.3
-
44
-
-
0036317297
-
Osteogenesis imperfecta type VII: An autosomal recessive form of brittle bone disease
-
Jul
-
Ward LM, Rauch F, Travers R, et al. (Jul. 2002) Osteogenesis imperfecta type VII: an autosomal recessive form of brittle bone disease. Bone 31(1):12-8.
-
(2002)
Bone
, vol.31
, Issue.1
, pp. 12-18
-
-
Ward, L.M.1
Rauch, F.2
Travers, R.3
-
45
-
-
0030754162
-
Osteogenesis imperfecta and other heritable disorders of bone
-
Paterson C (1997) Osteogenesis imperfecta and other heritable disorders of bone. Balliere's Clin Endo and Metabolism 11(1):195-209.
-
(1997)
Balliere's Clin Endo and Metabolism
, vol.11
, Issue.1
, pp. 195-209
-
-
Paterson, C.1
-
47
-
-
33646348736
-
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
-
Shore EM, Xu M, Feldman GJ, Fenstermacher DA, Consortium F O P I R, Brown MA, Kaplan FS (2006) A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nat Genet 38:525-527.
-
(2006)
Nat Genet
, vol.38
, pp. 525-527
-
-
Shore, E.M.1
Xu, M.2
Feldman, G.J.3
Fenstermacher, D.A.4
Consortium, F.O.P.I.R.5
Brown, M.A.6
Kaplan, F.S.7
-
48
-
-
0031964498
-
Catastrophic falls in patients who have fibrodysplasia ossificans progressiva
-
Glaser DL, Rocke DM, Kaplan FS (1998) Catastrophic falls in patients who have fibrodysplasia ossificans progressiva. Clin Orthop 346:110-116.
-
(1998)
Clin Orthop
, vol.346
, pp. 110-116
-
-
Glaser, D.L.1
Rocke, D.M.2
Kaplan, F.S.3
-
49
-
-
0034331685
-
Progressive osseous heteroplasia: A perspective
-
Kaplan, F. S. and E. M. Shore (2000). Progressive osseous heteroplasia: a perspective. J. Bone Min. Res. 15, 2084-2094.
-
(2000)
J. Bone Min. Res.
, vol.15
, pp. 2084-2094
-
-
Kaplan, F.S.1
Shore, E.M.2
-
50
-
-
0018292184
-
Kniest dysplasia. A histochemical study of the grown plate
-
November
-
Horton WA, Rimoin DL Kniest dysplasia. A histochemical study of the grown plate. Pediatr. Res. 1979 November 13(11):1266-70
-
(1979)
Pediatr. Res.
, vol.13
, Issue.11
, pp. 1266-1270
-
-
Horton, W.A.1
Rimoin, D.L.2
-
51
-
-
0032548931
-
Structurally abnormal type II collagen in a severe form of Kniest dysplasia caused by an exon 24 skipping mutation
-
Feb. 20. UI: 946
-
Weis MA. Wilkin DJ. Kim HJ. Wilcox WR. Lachman RS. Rimoin DL. Cohn DH. Eyre DR. Structurally abnormal type II collagen in a severe form of Kniest dysplasia caused by an exon 24 skipping mutation. [Journal Article. Research Support, U. S. Gov't, P. H. S.] Journal of Biological Chemistry. 273(8):4761-8, 1998 Feb. 20. UI: 946
-
(1998)
[Journal Article. Research Support, U. S. Gov't, P. H. S.] Journal of Biological Chemistry
, vol.273
, Issue.8
, pp. 4761-4768
-
-
Weis, M.A.1
Wilkin, D.J.2
Kim, H.J.3
Wilcox, W.R.4
Lachman, R.S.5
Rimoin, D.L.6
Cohn, D.H.7
Eyre, D.R.8
|