-
3
-
-
0028074557
-
Cleft hand/foot: Clinical and development aspects
-
Buss PW (1994). Cleft hand/foot: Clinical and development aspects. Journal of Medical Genetics, 31: 726-730.
-
(1994)
Journal of Medical Genetics
, vol.31
, pp. 726-730
-
-
Buss, P.W.1
-
4
-
-
0023513690
-
Classification of 578 cases of congenital upper limb anomalies with the IFSSH system - A 10 years' experience
-
Cheng JC, Chow SK, Leung PC (1987). Classification of 578 cases of congenital upper limb anomalies with the IFSSH system - A 10 years' experience. Journal of Hand Surgery, 12A: 1055-1060.
-
(1987)
Journal of Hand Surgery
, vol.12 A
, pp. 1055-1060
-
-
Cheng, J.C.1
Chow, S.K.2
Leung, P.C.3
-
5
-
-
0020992494
-
Family study of congenital limb reduction abnormalities in Hungary 1975-1977
-
Czeizel A, Bod M, Lenz W (1983). Family study of congenital limb reduction abnormalities in Hungary 1975-1977. Human Genetics, 65: 34-45.
-
(1983)
Human Genetics
, vol.65
, pp. 34-45
-
-
Czeizel, A.1
Bod, M.2
Lenz, W.3
-
6
-
-
0029026767
-
Absence of radius and ulna in mice lacking hoxa-11 and hoxd-11
-
Davis AP, Witte DP, Hsieh-Li HM, Potter SS, Capecchi MR (1995). Absence of radius and ulna in mice lacking hoxa-11 and hoxd-11. Nature, 375: 791-795.
-
(1995)
Nature
, vol.375
, pp. 791-795
-
-
Davis, A.P.1
Witte, D.P.2
Hsieh-Li, H.M.3
Potter, S.S.4
Capecchi, M.R.5
-
7
-
-
0030710584
-
Application of the IFSSH(3)-classification for congenital anomalies of the hand; Results and problems
-
De Smet L, Matton G, Monstrey S, Cambier E, Fabry G (1997). Application of the IFSSH(3)-classification for congenital anomalies of the hand; Results and problems. Acta Orthopaedica Belgica, 63: 182-188.
-
(1997)
Acta Orthopaedica Belgica
, vol.63
, pp. 182-188
-
-
De Smet, L.1
Matton, G.2
Monstrey, S.3
Cambier, E.4
Fabry, G.5
-
8
-
-
0015413947
-
Classification of congenital malformations of the hand and upper extremity
-
Entin M, Barsky A, Swanson A (1972). Classification of congenital malformations of the hand and upper extremity. Hand, 4: 215-219.
-
(1972)
Hand
, vol.4
, pp. 215-219
-
-
Entin, M.1
Barsky, A.2
Swanson, A.3
-
9
-
-
0008264229
-
Classification, incidence
-
In: Flatt AE (Ed.); St Louis, Quality Medical Publishing Inc.
-
Flatt AE. Classification, incidence. In: Flatt AE (Ed.) The Care of Congenital Hand Anomalies, 2nd edn. St Louis, Quality Medical Publishing Inc., 1994: 47-63.
-
(1994)
The Care of Congenital Hand Anomalies, 2nd edn.
, pp. 47-63
-
-
Flatt, A.E.1
-
10
-
-
0028273071
-
Congenital constriction band syndrome: A seventy-year experience
-
Folkes GD, Reinker K (1994). Congenital constriction band syndrome: A seventy-year experience. Journal of Pediatric Orthopaedics, 14: 242-248.
-
(1994)
Journal of Pediatric Orthopaedics
, vol.14
, pp. 242-248
-
-
Folkes, G.D.1
Reinker, K.2
-
12
-
-
0017370132
-
Descriptive system for congenital limb anomalies
-
Frias ML, Castilla EE, Paz JE (1977). Descriptive system for congenital limb anomalies. Teratology, 15: 163-169.
-
(1977)
Teratology
, vol.15
, pp. 163-169
-
-
Frias, M.L.1
Castilla, E.E.2
Paz, J.E.3
-
13
-
-
0027161731
-
Amniotic band sequence and limb defects: Data from a population-based study
-
Froster UG, Baird PA (1993). Amniotic band sequence and limb defects: Data from a population-based study. American Journal of Medical Genetics, 46: 497-500.
-
(1993)
American Journal of Medical Genetics
, vol.46
, pp. 497-500
-
-
Froster, U.G.1
Baird, P.A.2
-
15
-
-
0020383632
-
Congenital anomalies of the upper limb among the Chinese population in Hong Kong
-
Leung PC, Chan KM, Chen JC (1982). Congenital anomalies of the upper limb among the Chinese population in Hong Kong. Journal of Hand Surgery, 7A: 563-565.
-
(1982)
Journal of Hand Surgery
, vol.7 A
, pp. 563-565
-
-
Leung, P.C.1
Chan, K.M.2
Chen, J.C.3
-
17
-
-
0029117749
-
A duplicated zone of polarizing activity in polydactylous mouse mutants
-
Masuya H, Sagai T, Wakana S, Moriwaki K, Shiroishi T (1995). A duplicated zone of polarizing activity in polydactylous mouse mutants. Genes and Development, 9: 1645-1653.
-
(1995)
Genes and Development
, vol.9
, pp. 1645-1653
-
-
Masuya, H.1
Sagai, T.2
Wakana, S.3
Moriwaki, K.4
Shiroishi, T.5
-
18
-
-
0028307828
-
The position of symbrachydactyly in the classification of congenital hand anomalies
-
Miura T, Nakamura R, Horii E (1994). The position of symbrachydactyly in the classification of congenital hand anomalies. Journal of Hand Surgery, 19B: 350-354.
-
(1994)
Journal of Hand Surgery
, vol.19 B
, pp. 350-354
-
-
Miura, T.1
Nakamura, R.2
Horii, E.3
-
19
-
-
0026710927
-
Cleft hand, syndactyly and hypoplastic thumb
-
Miura T, Nakamura R, Suzuki M, Watanabe K (1992). Cleft hand, syndactyly and hypoplastic thumb. Journal of Hand Surgery, 17B: 365-370.
-
(1992)
Journal of Hand Surgery
, vol.17 B
, pp. 365-370
-
-
Miura, T.1
Nakamura, R.2
Suzuki, M.3
Watanabe, K.4
-
20
-
-
0031762875
-
Congenital hand problems. Terminology, etiology, and management
-
Netscher DT (1998). Congenital hand problems. Terminology, etiology, and management. Clinics in Plastic Surgery, 25: 537-552.
-
(1998)
Clinics in Plastic Surgery
, vol.25
, pp. 537-552
-
-
Netscher, D.T.1
-
21
-
-
0022802297
-
Congenital anomalies of the upper limb among the Japanese in Sapporo
-
Ogino T, Minami A, Fukuda K, Kato H (1986). Congenital anomalies of the upper limb among the Japanese in Sapporo. Journal of Hand Surgery, 11B: 364-371.
-
(1986)
Journal of Hand Surgery
, vol.11 B
, pp. 364-371
-
-
Ogino, T.1
Minami, A.2
Fukuda, K.3
Kato, H.4
-
22
-
-
0023634216
-
Congenital constriction band syndrome and transverse deficiency
-
Ogino T, Saitou Y (1987). Congenital constriction band syndrome and transverse deficiency. Journal of Hand Surgery, 12B: 343-348.
-
(1987)
Journal of Hand Surgery
, vol.12 B
, pp. 343-348
-
-
Ogino, T.1
Saitou, Y.2
-
23
-
-
0021901484
-
The development and classification of anomalies of the limbs in the human
-
O'Rahilly R (1985). The development and classification of anomalies of the limbs in the human. Progress in Clinical and Biological Research, 163C: 85-90.
-
(1985)
Progress in Clinical and Biological Research
, vol.163 C
, pp. 85-90
-
-
O'Rahilly, R.1
-
24
-
-
0030782397
-
Polydactyly and ectopic ZPA formation in Alx-4 mutant mice
-
Qu S, Niswender KD, Ji Q et al. (1997). Polydactyly and ectopic ZPA formation in Alx-4 mutant mice. Development, 124: 3999-4008.
-
(1997)
Development
, vol.124
, pp. 3999-4008
-
-
Qu, S.1
Niswender, K.D.2
Ji, Q.3
-
25
-
-
0029097168
-
In vitro model of syndactyly replicates the morphologic features observed in vivo
-
Stafford DL, Lussier MR, Sank AC, Shuler CF (1995). In vitro model of syndactyly replicates the morphologic features observed in vivo. Plastic and Reconstructive Surgery, 96: 1169-1176.
-
(1995)
Plastic and Reconstructive Surgery
, vol.96
, pp. 1169-1176
-
-
Stafford, D.L.1
Lussier, M.R.2
Sank, A.C.3
Shuler, C.F.4
-
27
-
-
0025022620
-
Mirror polydactyly: Pathogenesis based on a morphogen gradient theory
-
[see comments]
-
Viljoen DL, Kidson SH (1990). Mirror polydactyly: Pathogenesis based on a morphogen gradient theory [see comments]. American Journal of Medical Genetics, 35: 229-235.
-
(1990)
American Journal of Medical Genetics
, vol.35
, pp. 229-235
-
-
Viljoen, D.L.1
Kidson, S.H.2
-
28
-
-
0025293319
-
Cocaine as a cause of congenital malformations of vascular origin: Experimental evidence in the rat
-
Webster WS, Brown-Woodman PD (1990). Cocaine as a cause of congenital malformations of vascular origin: Experimental evidence in the rat. Teratology, 41: 689-697.
-
(1990)
Teratology
, vol.41
, pp. 689-697
-
-
Webster, W.S.1
Brown-Woodman, P.D.2
-
29
-
-
0027831551
-
Syndactylies and polydactylies: Embryological overview and suggested classification
-
Winter RM, Tickle C (1993). Syndactylies and polydactylies: Embryological overview and suggested classification. European Journal of Human Genetics, 1: 96-104.
-
(1993)
European Journal of Human Genetics
, vol.1
, pp. 96-104
-
-
Winter, R.M.1
Tickle, C.2
-
30
-
-
0032961403
-
Clinical and genetic studies on 12 preaxial polydactyly families and refinement of the localisation of the gene responsible to a 1.9 cM region on chromosome 7q36
-
Zguricas J, Heus H, Morales-Peralta E et al. (1999). Clinical and genetic studies on 12 preaxial polydactyly families and refinement of the localisation of the gene responsible to a 1.9 cM region on chromosome 7q36. Journal of Medical Genetics, 36: 32-40.
-
(1999)
Journal of Medical Genetics
, vol.36
, pp. 32-40
-
-
Zguricas, J.1
Heus, H.2
Morales-Peralta, E.3
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