-
1
-
-
0000979928
-
Mental retardation with osteocartilaginous anomalies
-
Coffin GS, Siris E, Wegienka LC: Mental retardation with osteocartilaginous anomalies. Am J Dis Child 1966,112:205-213.
-
(1966)
Am J Dis Child
, vol.112
, pp. 205-213
-
-
Coffin, G.S.1
Siris, E.2
Wegienka, L.C.3
-
2
-
-
0015073716
-
A new dominant gene mental retardation syndrome
-
Lowry B, Miller JR, Fraser FC: A new dominant gene mental retardation syndrome. Am J Dis Child 1971;121:491-500.
-
(1971)
Am J Dis Child
, vol.121
, pp. 491-500
-
-
Lowry, B.1
Miller, J.R.2
Fraser, F.C.3
-
3
-
-
0023945707
-
The Coffin-Lowry syndrome
-
Young ID: The Coffin-Lowry syndrome. J Med Genet 1988;25:344-348.
-
(1988)
J Med Genet
, vol.25
, pp. 344-348
-
-
Young, I.D.1
-
4
-
-
0020079421
-
The Coffin-Lowry syndrome: Experience from four centres
-
Hunter AGW, Partington MW, Evans JA: The Coffin-Lowry syndrome: Experience from four centres. Clin Genet 1982;21:321-335.
-
(1982)
Clin Genet
, vol.21
, pp. 321-335
-
-
Hunter, A.G.W.1
Partington, M.W.2
Evans, J.A.3
-
5
-
-
0015384319
-
Mental retardation, abnormal fingers, and skeletal anomalies: Coffin's syndrome
-
Procopis PG, Turner B: Mental retardation, abnormal fingers, and skeletal anomalies: Coffin's syndrome. Am J Dis Child 1972;124:258-261.
-
(1972)
Am J Dis Child
, vol.124
, pp. 258-261
-
-
Procopis, P.G.1
Turner, B.2
-
6
-
-
0028068827
-
Construction of a high-resolution linkage map for Xp22.I-p22.2 and refinement of the genetic localisation of the Coffin-Lowry syndrome gene
-
Biancalana V, Trivier E, Weber C, Weissenbach J, Rowe PS, O'Riordan JL, Partington MW: Construction of a high-resolution linkage map for Xp22.I-p22.2 and refinement of the genetic localisation of the Coffin-Lowry syndrome gene. Genomics 1994:22:617-625.
-
(1994)
Genomics
, vol.22
, pp. 617-625
-
-
Biancalana, V.1
Trivier, E.2
Weber, C.3
Weissenbach, J.4
Rowe, P.S.5
O'Riordan, J.L.6
Partington, M.W.7
-
7
-
-
0023680453
-
A family with the Coffin-Lowry syndrome revisited: Localization of CLS to Xp21-pter
-
Partington MW, Mulley JC, Sutherland GR, Thode A, Turner G: A family with the Coffin-Lowry syndrome revisited: Localization of CLS to Xp21-pter. Am J Med Genet 1988;30: 509-521.
-
(1988)
Am J Med Genet
, vol.30
, pp. 509-521
-
-
Partington, M.W.1
Mulley, J.C.2
Sutherland, G.R.3
Thode, A.4
Turner, G.5
-
8
-
-
0016812249
-
The Coffin-Lowry syndrome: An inherited faciodigital mental retardation syndrome
-
Tentamy SA, Miller JD, Hussels-Maumenee I: The Coffin-Lowry syndrome: An inherited faciodigital mental retardation syndrome. J Pediatr 1985;86:724-731.
-
(1985)
J Pediatr
, vol.86
, pp. 724-731
-
-
Tentamy, S.A.1
Miller, J.D.2
Hussels-Maumenee, I.3
-
9
-
-
0003539147
-
-
Oxford, Oxford University Press
-
Gorlin RJ, Toriello HV, Cohen MM: Hereditary Hearing Loss and Its Syndromes. Oxford, Oxford University Press, 1995, pp 421-422.
-
(1995)
Hereditary Hearing Loss and Its Syndromes
, pp. 421-422
-
-
Gorlin, R.J.1
Toriello, H.V.2
Cohen, M.M.3
-
10
-
-
0027475725
-
Pleiotropy in Coffin-Lowry syndrome: Sensorineural hearing deficit and premature tooth loss as early manifestations
-
Hartsfield JK, Hall BD, Grix AW, Koussef BG, Salazar JF, Haufe SMW: Pleiotropy in Coffin-Lowry syndrome: Sensorineural hearing deficit and premature tooth loss as early manifestations. Am J Med Genet 1993;45:552-557.
-
(1993)
Am J Med Genet
, vol.45
, pp. 552-557
-
-
Hartsfield, J.K.1
Hall, B.D.2
Grix, A.W.3
Koussef, B.G.4
Salazar, J.F.5
Haufe, S.M.W.6
-
11
-
-
0028348804
-
Coffin-Lowry syndrome with sensorineural deafness and labyrinthine anomaly
-
Higashi K, Matsuki C: Coffin-Lowry syndrome with sensorineural deafness and labyrinthine anomaly. J Laryngol Otol 1994;108:147-148.
-
(1994)
J Laryngol Otol
, vol.108
, pp. 147-148
-
-
Higashi, K.1
Matsuki, C.2
-
12
-
-
0021742219
-
The Coffin-Lowry syndrome: A study of two new index patients and their families
-
Haspeslagh M, Fryns JP, Beusen L, Van Dessel F, Vinken L, Moens E, Van Den Berghe H: The Coffin-Lowry syndrome: A study of two new index patients and their families. Eur J Pediatr 1984;143:82-86.
-
(1984)
Eur J Pediatr
, vol.143
, pp. 82-86
-
-
Haspeslagh, M.1
Fryns, J.P.2
Beusen, L.3
Van Dessel, F.4
Vinken, L.5
Moens, E.6
Van Den Berghe, H.7
-
13
-
-
0019456679
-
Early recognition of the Coffin-Lowry syndrome
-
Wilson WG, Kelly TE: Early recognition of the Coffin-Lowry syndrome. Am J Med Genet 1981;8:215-220.
-
(1981)
Am J Med Genet
, vol.8
, pp. 215-220
-
-
Wilson, W.G.1
Kelly, T.E.2
|