-
1
-
-
0014572153
-
Frontometnphyscal dysplasia: A new syndrome
-
Gorlin, R. J., and Cohen, M. M.,Jr. Frontometnphyscal dysplasia: A new syndrome. Am.]. Dis. Child. 118: 487, 1969.
-
(1969)
Am.. Dis. Child.
, vol.118
, pp. 487
-
-
Gorlin, R.J.1
Cohen Jr., M.M.2
-
2
-
-
0021717758
-
Frontometaphyseal dysplasia: Symptoms and possible mode of inheritance
-
Jend-Rossmann, I.,Jend, H. H., Ringe.J. D., et al. Frontometaphyseal dysplasia: Symptoms and possible mode of inheritance.J. Oral Maxillofac, Snrg. 42: 743, 1984.
-
(1984)
J. Oral Maxillofac, Snrg.
, vol.42
, pp. 743
-
-
Jend-Rossmann, I.1
Jend, H.H.2
Ringe, J.D.3
-
3
-
-
84907113531
-
Ophthalmological complications in the sclerosing bone dysplasias
-
Beighton, P., and Hamersma, H. Ophthalmological complications in the sclerosing bone dysplasias. Ophthalmic Paediatr. Genet. 6: 129, 1995.
-
(1995)
Ophthalmic Paediatr. Genet.
, vol.6
, pp. 129
-
-
Beighton, P.1
Hamersma, H.2
-
4
-
-
0022535895
-
Mitral valve prolapse in a patient with frontometaphyseal dysplasia
-
Park, J. M., Contreras, E. A., and Garcia, R. R. Mitral valve prolapse in a patient with frontometaphyseal dysplasia. Clin. Pedialr. 25: 469, 1986.
-
(1986)
Clin. Pedialr.
, vol.25
, pp. 469
-
-
Park, J.M.1
Contreras, E.A.2
Garcia, R.R.3
-
5
-
-
0023854782
-
Laryngo-tracheal stenosis in frontometaphyseal dysplasia
-
Leggett, J. M. Laryngo-tracheal stenosis in frontometaphyseal dysplasia J Laryngol. Otol. 102: 74, 1988.
-
(1988)
J Laryngol. Otol.
, vol.102
, pp. 74
-
-
Leggett, J.M.1
-
6
-
-
0023772657
-
The anaesthetic management of an infant with frontometaphyseal dysplasia (GorlinCohen syndrome)
-
Mehta.Y., and Schon, H. The anaesthetic management of an infant with frontometaphyseal dysplasia (GorlinCohen syndrome). Ada Anaestliesiol. Scand. 32: 505, 1988.
-
(1988)
Ada Anaestliesiol. Scand.
, vol.32
, pp. 505
-
-
MehtaY1
Schon, H.2
-
7
-
-
12044257698
-
Sibs with mental retardation, supraorbital sclerosis, and metaphyseal clysplasia: Frontometaphyseal dysplasia, craniometaphyseal dysplasia, or a new syndrome?
-
Reardon, W., Hall, C. M., Dillon, M. J., et al. Sibs with mental retardation, supraorbital sclerosis, and metaphyseal clysplasia: Frontometaphyseal dysplasia, craniometaphyseal dysplasia, or a new syndrome? J Med. Genet. 28: 622, 1991.
-
(1991)
J Med. Genet.
, vol.28
, pp. 622
-
-
Reardon, W.1
Hall, C.M.2
Dillon, M.J.3
-
8
-
-
0027415127
-
Restrictive chest bellows disease and frontometaphyscal dysplasia
-
Lipson, E., Ahmed, T., Kiel, M. H., et al. Restrictive chest bellows disease and frontometaphyscal dysplasia. Chest 103: 1264, 1993.
-
(1993)
Chest
, vol.103
, pp. 1264
-
-
Lipson, E.1
Ahmed, T.2
Kiel, M.H.3
-
9
-
-
0029061195
-
Frontometaphyseal dysplasia: Neonatal radiographie diagnosis
-
Glass, R. B.J., and Rosenbattm, K. N. Frontometaphyseal dysplasia: Neonatal radiographie diagnosis. Am.J. Med. Genet. 57: 1, 1995.
-
(1995)
Am.J. Med. Genet.
, vol.57
, pp. 1
-
-
Glass, R.B.J.1
Rosenbattm, K.N.2
-
10
-
-
0029558257
-
Radiographic changes of frontometaphyseal dysplasia in the neonate
-
Nishimura, G., Takano, H., Aihara, T., et al. Radiographic changes of frontometaphyseal dysplasia in the neonate. Pedialr. Radial 25: S143, 1995.
-
(1995)
Pedialr. Radial
, vol.25
-
-
Nishimura, G.1
Takano, H.2
Aihara, T.3
-
11
-
-
0018936191
-
Frontometaphyseal dysplasia: Evidence for X-linked inheritance. J
-
Gorlin, R.J., and Winter, R. B. Frontometaphyseal dysplasia: Evidence for X-linked inheritance. J Med. Genet. 5: 81, 1980.
-
(1980)
Med. Genet.
, vol.5
, pp. 81
-
-
Gorlin, R.J.1
Winter, R.B.2
-
12
-
-
0003868876
-
-
New York: Oxford University Press
-
Gorlin, R.J., Cohen, M. M., and Levin, L. S. Syndromes of the Head and Neck. Third Ed., New York: Oxford University Press, 1990.
-
(1990)
Syndromes of the Head and Neck Third Ed.
-
-
Gorlin, R.J.1
Cohen, M.M.2
Levin, L.S.3
-
13
-
-
0015981710
-
Otolaryngologic manifestations of frontometaphyseal dysplasia: The Gorlin-Holt syndrome
-
Arenberg, I. K., Shambaugh, G. E., Jr., and Valvassori, G. E. Otolaryngologic manifestations of frontometaphyseal dysplasia: The Gorlin-Holt syndrome. Arch. Otolaryngol. 99: 52, 1974.
-
(1974)
Arch. Otolaryngol.
, vol.99
, pp. 52
-
-
Arenberg, I.K.1
Shambaugh, G.E.2
Jr3
Valvassori, G.E.4
-
14
-
-
0016719956
-
Frontometaphyseal dysplasia: Evidence for dominant inheritance
-
Weiss, L., Reynolds, W. A., and Szymanowski, R. T. Frontometaphyseal dysplasia: Evidence for dominant inheritance. Birth Defects 11: 55, 1975.
-
(1975)
Birth Defects
, vol.11
, pp. 55
-
-
Weiss, L.1
Reynolds, W.A.2
Szymanowski, R.T.3
-
15
-
-
0018593642
-
Frontometaphyseal dysplasia with congenital urinary tract malformations
-
Kanemura, T., Orii,T.,andOhtani,M. Frontometaphyseal dysplasia with congenital urinary tract malformations. Clin. Genet. 16: 399, 1979.
-
(1979)
Clin. Genet.
, vol.16
, pp. 399
-
-
Kanemura, T.1
Orii, T.2
Ohtani, M.3
|