-
1
-
-
0033724706
-
Replication timing of homologous alpha-satellite DNA in Roberts syndrome
-
Barbosa AC, Otto PA, Vianna-Morgante AM, 2000. Replication timing of homologous alpha-satellite DNA in Roberts syndrome. Chromosome Res 8(7): 645-650.
-
(2000)
Chromosome Res
, vol.8
, Issue.7
, pp. 645-650
-
-
Barbosa, A.C.1
Otto, P.A.2
Vianna-Morgante, A.M.3
-
2
-
-
0034639304
-
Further case of aminopterin syndrome sine aminopterin in a Spanish child
-
Garcia-Minaur S, Botella MP. 2000. Further case of aminopterin syndrome sine aminopterin in a Spanish child. Am J Med Genet 95(4): 320-324.
-
(2000)
Am J Med Genet
, vol.95
, Issue.4
, pp. 320-324
-
-
Garcia-Minaur, S.1
Botella, M.P.2
-
3
-
-
0141857858
-
Juberg-Hayward syndrome: Report of a new patient with severe phenotype and novel clinical features
-
Hedera P, Innis JW. 2003. Juberg-Hayward syndrome: report of a new patient with severe phenotype and novel clinical features. Am J Med Genet 122A(3): 257-260.
-
(2003)
Am J Med Genet
, vol.122 A
, Issue.3
, pp. 257-260
-
-
Hedera, P.1
Innis, J.W.2
-
4
-
-
0014508405
-
A new familial syndrome of oral, cranial, and digital anomalies
-
Juberg RC, Hayward JR. 1969. A new familial syndrome of oral, cranial, and digital anomalies. J Pediatr 74(5): 755-762.
-
(1969)
J Pediatr
, vol.74
, Issue.5
, pp. 755-762
-
-
Juberg, R.C.1
Hayward, J.R.2
-
5
-
-
0032939016
-
Juberg-Hayward syndrome: A new case report and clinical delineation of the syndrome
-
Kantaputra PN, Mongkolchaisup S. 1999. Juberg-Hayward syndrome: a new case report and clinical delineation of the syndrome. Clin Dysmorphol 8(2): 123-127.
-
(1999)
Clin Dysmorphol
, vol.8
, Issue.2
, pp. 123-127
-
-
Kantaputra, P.N.1
Mongkolchaisup, S.2
-
6
-
-
0019973502
-
Orocraniodigital (Juberg-Hayward) syndrome with growth hormone deficiency
-
Kingston HM, Hughes IA, Harper PS. 1982. Orocraniodigital (Juberg-Hayward) syndrome with growth hormone deficiency. Arch Dis Child 57(10): 790-792.
-
(1982)
Arch Dis Child
, vol.57
, Issue.10
, pp. 790-792
-
-
Kingston, H.M.1
Hughes, I.A.2
Harper, P.S.3
-
7
-
-
0021015544
-
A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies
-
Malpuech G, Demeocq F, Palcoux JB, Vanlieferinghen P. 1983. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies. Am J Med Genet 16(4): 475-480.
-
(1983)
Am J Med Genet
, vol.16
, Issue.4
, pp. 475-480
-
-
Malpuech, G.1
Demeocq, F.2
Palcoux, J.B.3
Vanlieferinghen, P.4
-
8
-
-
0019854435
-
A case of the orocraniodigital (Juberg-Hayward) syndrome
-
Nevin NC, Henry P, Thomas PT. 1981. A case of the orocraniodigital (Juberg-Hayward) syndrome. J Med Genet 18(6): 478-481.
-
(1981)
J Med Genet
, vol.18
, Issue.6
, pp. 478-481
-
-
Nevin, N.C.1
Henry, P.2
Thomas, P.T.3
-
9
-
-
0035076379
-
An atypical case suggesting the possibility of overlap between Malpuech and Juberg-Hayward syndromes
-
Reardon W, Hall CM, Gorman W. 2001. An atypical case suggesting the possibility of overlap between Malpuech and Juberg-Hayward syndromes. Clin Dysmorphol 10(2): 123-128.
-
(2001)
Clin Dysmorphol
, vol.10
, Issue.2
, pp. 123-128
-
-
Reardon, W.1
Hall, C.M.2
Gorman, W.3
-
10
-
-
0034120489
-
Juberg-Hayward syndrome: Report of a case with cleft palate, distally placed thumbs and vertebral anomalies
-
Silengo M, Tornetta L. 2000. Juberg-Hayward syndrome: report of a case with cleft palate, distally placed thumbs and vertebral anomalies. Clin Dysmorphol 9(2): 127-129.
-
(2000)
Clin Dysmorphol
, vol.9
, Issue.2
, pp. 127-129
-
-
Silengo, M.1
Tornetta, L.2
-
12
-
-
0026593993
-
The orocraniodigital syndrome of Juberg and Hayward
-
Verloes A, Le Merrer M, Davin JC, et al. 1992. The orocraniodigital syndrome of Juberg and Hayward. J Med Genet 29(4): 262-265.
-
(1992)
J Med Genet
, vol.29
, Issue.4
, pp. 262-265
-
-
Verloes, A.1
Le Merrer, M.2
Davin, J.C.3
|