-
2
-
-
0016314137
-
Morquio's syndrome. Deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfatase
-
Matalon R, Arbogast B, Justice P, Brandt P, Brandt Ek, Dorfman A. Morquio's syndrome. Deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfatase. Biochem Biophys Res Commun 1974; 61 : 759.
-
(1974)
Biochem Biophys Res Commun
, vol.61
, pp. 759
-
-
Matalon, R.1
Arbogast, B.2
Justice, P.3
Brandt, P.4
Brandt, E.5
Dorfman, A.6
-
3
-
-
0018828194
-
MPS IV B associated with β-galactosidase deficiency. Report of two cases
-
Groebe H, Krins M, Schmidberger H, Von Figura K, Harzer K et al. MPS IV B associated with β-galactosidase deficiency. Report of two cases. Am J Hum Genet 1980; 32 : 258.
-
(1980)
Am J Hum Genet
, vol.32
, pp. 258
-
-
Groebe, H.1
Krins, M.2
Schmidberger, H.3
Von Figura, K.4
Harzer, K.5
-
4
-
-
0021038696
-
Morquio B syndrome: A primary defect in β-galactosidase
-
Van der Horst GTJ, Kleijer WJ, Hoogeveen AT, Huijmans JGM, Blom W, Van Diggelen OP. Morquio B syndrome: A primary defect in β-galactosidase. Am J Med Genet 1983; 16 : 261.
-
(1983)
Am J Med Genet
, vol.16
, pp. 261
-
-
Van Der Horst, G.T.J.1
Kleijer, W.J.2
Hoogeveen, A.T.3
Huijmans, J.G.M.4
Blom, W.5
Van Diggelen, O.P.6
-
5
-
-
0023550148
-
Morquio's disease type B (β-galactosidase deficiency) in three siblings
-
Beck M, Pefersen EM, Spranger J, Beighton P. Morquio's disease type B (β-galactosidase deficiency) in three siblings. Afr Med J 1987; 72: 704.
-
(1987)
Afr Med J
, vol.72
, pp. 704
-
-
Beck, M.1
Pefersen, E.M.2
Spranger, J.3
Beighton, P.4
-
6
-
-
0017169884
-
Spondyloepiphyseal dysplasia, Corneal clouding, Normal intelligence and acid β-Galactosidase deficiency
-
O'Brien JS, Gugler E, Giedson A, Wiesmann U, Herschkowitz N, Meier C, Leroy J. Spondyloepiphyseal dysplasia, Corneal clouding, Normal intelligence and acid β-Galactosidase deficiency. Clin Genet 1976; 9 : 495.
-
(1976)
Clin Genet
, vol.9
, pp. 495
-
-
O'Brien, J.S.1
Gugler, E.2
Giedson, A.3
Wiesmann, U.4
Herschkowitz, N.5
Meier, C.6
Leroy, J.7
-
7
-
-
0020501856
-
Morquio B disease, Spondyloepiphyseal dysplasia associated with acid β-Galactosidase deficiency. Report of three cases in one family
-
Van Gemund JJ, Giesberts MAH, Eerdmans RF, Blom W, Kleijer WJ. Morquio B disease, Spondyloepiphyseal dysplasia associated with acid β-Galactosidase deficiency. Report of three cases in one family. Human Genet 1983; 64 : 50.
-
(1983)
Human Genet
, vol.64
, pp. 50
-
-
Van Gemund, J.J.1
Giesberts, M.A.H.2
Eerdmans, R.F.3
Blom, W.4
Kleijer, W.J.5
-
8
-
-
0017729343
-
Morquio like syndrome with β-Galactosidase deficiency & normal hexosamine sulfatase activity: Mucopolysaccharidosis IV B
-
Arbisser AI, Donnelly KA, Scott CI Jr, Diferrante NM, Singh J, Sterenson RE et al. Morquio like syndrome with β-Galactosidase deficiency & normal hexosamine sulfatase activity: mucopolysaccharidosis IV B. Am J Med Genet 1977; 1 : 195-205.
-
(1977)
Am J Med Genet
, vol.1
, pp. 195-205
-
-
Arbisser, A.I.1
Donnelly, K.A.2
Scott C.I., Jr.3
Diferrante, N.M.4
Singh, J.5
Sterenson, R.E.6
-
9
-
-
0023193081
-
Progressive mental regression in siblings with morquio disease type B
-
Giugliani R, Jackson M, Skinner SJ, Vimal CM, Fensom AH, Fahmy N et al. Progressive mental regression in siblings with morquio disease type B. Clin Genet 1987; 32 : 313.
-
(1987)
Clin Genet
, vol.32
, pp. 313
-
-
Giugliani, R.1
Jackson, M.2
Skinner, S.J.3
Vimal, C.M.4
Fensom, A.H.5
Fahmy, N.6
|