-
1
-
-
0027522655
-
Oral-facial-digital syndromes, 1992
-
Toriello HV. Oral-facial-digital syndromes, 1992. Clin Dysmorphol 1993;2:95-105.
-
(1993)
Clin Dysmorphol
, vol.2
, pp. 95-105
-
-
Toriello, H.V.1
-
2
-
-
0014102315
-
Genetic and clinical heterogeneity in the oral-facial-digital syndromes
-
Rimoin D, Edgerton M. Genetic and clinical heterogeneity in the oral-facial-digital syndromes. J Pediatr 1967;71:94-102.
-
(1967)
J Pediatr
, vol.71
, pp. 94-102
-
-
Rimoin, D.1
Edgerton, M.2
-
3
-
-
0017764274
-
Heart malformation as a feature of the Mohr syndrome
-
Cordero JF, Holmes LB. Heart malformation as a feature of the Mohr syndrome. J Pediatr 1977;91:683-4.
-
(1977)
J Pediatr
, vol.91
, pp. 683-684
-
-
Cordero, J.F.1
Holmes, L.B.2
-
6
-
-
0026690316
-
Congenital heart defects, hamartomas of the tongue and polysyndactyly in a sister and brother
-
Orstavik KH, Lindemann R, Solberg LA, Foerster A, Sorland SJ. Congenital heart defects, hamartomas of the tongue and polysyndactyly in a sister and brother. Clin Genet 1992;42:19-21.
-
(1992)
Clin Genet
, vol.42
, pp. 19-21
-
-
Orstavik, K.H.1
Lindemann, R.2
Solberg, L.A.3
Foerster, A.4
Sorland, S.J.5
-
7
-
-
0029033284
-
Joint dislocation and cerebral anomalies are consistently associated with oral-facial-digital syndrome type IV
-
Digilio MC, Giannotti A, Pagnotta G, Mingarelli R, Dallapiccola B. Joint dislocation and cerebral anomalies are consistently associated with oral-facial-digital syndrome type IV. Clin Genet 1995;48:156-9.
-
(1995)
Clin Genet
, vol.48
, pp. 156-159
-
-
Digilio, M.C.1
Giannotti, A.2
Pagnotta, G.3
Mingarelli, R.4
Dallapiccola, B.5
-
8
-
-
0018878503
-
Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies
-
Vàradi V, Szabò L, Papp Z. Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies. J Med Genet 1980;17:119-22.
-
(1980)
J Med Genet
, vol.17
, pp. 119-122
-
-
Vàradi, V.1
Szabò, L.2
Papp, Z.3
-
9
-
-
0015187961
-
Syndrome characterized by lingual malformation, polydactyly, tachypnea, and psychomotor retardation (Mohr syndrome)
-
Gustavson KH, Kreuger A, Petersson PO. Syndrome characterized by lingual malformation, polydactyly, tachypnea, and psychomotor retardation (Mohr syndrome). Clin Genet 1971;2:261-6.
-
(1971)
Clin Genet
, vol.2
, pp. 261-266
-
-
Gustavson, K.H.1
Kreuger, A.2
Petersson, P.O.3
-
10
-
-
0025208291
-
Orofaciodigital syndrome type IV (Mohr-Majewski syndrome) with severe expression expanding the known spectrum of anomalies
-
Meinecke P, Hayek H. Orofaciodigital syndrome type IV (Mohr-Majewski syndrome) with severe expression expanding the known spectrum of anomalies. J Med Genet 1990;27:200-2.
-
(1990)
J Med Genet
, vol.27
, pp. 200-202
-
-
Meinecke, P.1
Hayek, H.2
-
11
-
-
0017367343
-
A postaxial polydactyly-dental-vertebral syndrome
-
Rogers JG, Levin LS, Dorst JP, Temtamy SA. A postaxial polydactyly-dental-vertebral syndrome, J Pediatr 1977;90:230-5.
-
(1977)
J Pediatr
, vol.90
, pp. 230-235
-
-
Rogers, J.G.1
Levin, L.S.2
Dorst, J.P.3
Temtamy, S.A.4
-
12
-
-
0020591263
-
The Mohr syndrome: Are there two variants?
-
Haumont D, Pelc S. The Mohr syndrome: are there two variants? Clin Genet 1983;24:41-6.
-
(1983)
Clin Genet
, vol.24
, pp. 41-46
-
-
Haumont, D.1
Pelc, S.2
-
13
-
-
0027960418
-
Oral-facial-digital syndrome: Report on a transitional type between the Mohr and Vàradi syndromes in a fetus
-
Camera G, Marasini M, Pozzolo S, Camera A. Oral-facial-digital syndrome: report on a transitional type between the Mohr and Vàradi syndromes in a fetus. Am J Med Genet 1994;53:196-8.
-
(1994)
Am J Med Genet
, vol.53
, pp. 196-198
-
-
Camera, G.1
Marasini, M.2
Pozzolo, S.3
Camera, A.4
-
14
-
-
0027423379
-
Congenital heart disease in patients with Down's syndrome: Anatomic and genetic aspects
-
Marino B. Congenital heart disease in patients with Down's syndrome: anatomic and genetic aspects. Biomed Pharmacother 1993;47:197-200.
-
(1993)
Biomed Pharmacother
, vol.47
, pp. 197-200
-
-
Marino, B.1
-
15
-
-
0026583504
-
Nonrandom association of atrioventricular canal and del(8p) syndrome
-
Marino B, Reale A, Giannotti A, Digilio MC, Dallapiccola B. Nonrandom association of atrioventricular canal and del(8p) syndrome. Am J Med Genet 1992;42:424-7.
-
(1992)
Am J Med Genet
, vol.42
, pp. 424-427
-
-
Marino, B.1
Reale, A.2
Giannotti, A.3
Digilio, M.C.4
Dallapiccola, B.5
-
16
-
-
0029655165
-
Atrioventricular canal and 3C (cranio-cerebello-cardiac) syndrome
-
Digilio MC, Marino B, Giannotti A, Mingarelli R, Dallapiccola B. Atrioventricular canal and 3C (cranio-cerebello-cardiac) syndrome. Am J Med Genet 1995;58:97-8.
-
(1995)
Am J Med Genet
, vol.58
, pp. 97-98
-
-
Digilio, M.C.1
Marino, B.2
Giannotti, A.3
Mingarelli, R.4
Dallapiccola, B.5
-
19
-
-
0014232741
-
Congenital heart disease and chondroectodermal dysplasia. Report of two cases, one in a Negro
-
Lynch JI, Perry LW, Takakuwa T, Scott LP. Congenital heart disease and chondroectodermal dysplasia. Report of two cases, one in a Negro. Am J Dis Child 1968;115:80-7.
-
(1968)
Am J Dis Child
, vol.115
, pp. 80-87
-
-
Lynch, J.I.1
Perry, L.W.2
Takakuwa, T.3
Scott, L.P.4
-
20
-
-
0029353380
-
Single atrium, atrioventricular canal/postaxial hexodactyly indicating Ellis-van Creveld syndrome
-
Digilio MC, Marino B, Giannotti A, Dallapiccola B. Single atrium, atrioventricular canal/postaxial hexodactyly indicating Ellis-van Creveld syndrome. Hum Genet 1995;96:251-3.
-
(1995)
Hum Genet
, vol.96
, pp. 251-253
-
-
Digilio, M.C.1
Marino, B.2
Giannotti, A.3
Dallapiccola, B.4
-
22
-
-
85005129184
-
-
New York: Alan R Liss for the National Foundation - March of Dimes. Birth Defects
-
Temtamy S, McKusick VA. The genetics of hand malformations. 2nd ed. New York: Alan R Liss for the National Foundation - March of Dimes. Birth Defects 1978;XIV(3):431-7.
-
(1978)
The Genetics of Hand Malformations. 2nd Ed.
, vol.14
, Issue.3
, pp. 431-437
-
-
Temtamy, S.1
McKusick, V.A.2
-
23
-
-
0023954590
-
Oro-facial-digital syndrome type II
-
Gillerot Y. Oro-facial-digital syndrome type II. Clin Genet 1988;33:140-3.
-
(1988)
Clin Genet
, vol.33
, pp. 140-143
-
-
Gillerot, Y.1
-
24
-
-
0024596804
-
Orofaciodigital syndrome type IV: Report of a patient
-
Nevin NC, Thomas PS. Orofaciodigital syndrome type IV: report of a patient. Am J Med Genet 1989;32:151-1.
-
(1989)
Am J Med Genet
, vol.32
, pp. 151-151
-
-
Nevin, N.C.1
Thomas, P.S.2
|