-
1
-
-
0028041418
-
Ectopic expression of Hoxb-8 causes duplication of the ZPA in the forelimb and homeotic transformation of axial structures
-
Charité J, Graaf W de, Shen S, Deschamps J (1994) Ectopic expression of Hoxb-8 causes duplication of the ZPA in the forelimb and homeotic transformation of axial structures. Cell 78: 589-601
-
(1994)
Cell
, vol.78
, pp. 589-601
-
-
Charité, J.1
De Graaf, W.2
Shen, S.3
Deschamps, J.4
-
2
-
-
0025797513
-
Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5
-
Chisaka O, Capecchi MR (1991) Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5. Nature 350: 473-479
-
(1991)
Nature
, vol.350
, pp. 473-479
-
-
Chisaka, O.1
Capecchi, M.R.2
-
3
-
-
0016176846
-
The Roberts syndrome
-
Freeman MV, Williams DW, Schmike RN, Temtamy SA, Vachier E, German J (1974) The Roberts syndrome. Clin Genet 5: 1-16
-
(1974)
Clin Genet
, vol.5
, pp. 1-16
-
-
Freeman, M.V.1
Williams, D.W.2
Schmike, R.N.3
Temtamy, S.A.4
Vachier, E.5
German, J.6
-
5
-
-
0026734111
-
Pax in development
-
Gruss P, Walther C (1992) Pax in development. Cell 69: 719-722
-
(1992)
Cell
, vol.69
, pp. 719-722
-
-
Gruss, P.1
Walther, C.2
-
6
-
-
0025289046
-
The Baller-Gerold syndrome: Phenotypic and cytogenetic overlap with Roberts syndrome
-
Huson SM, Rodgers CS, Hall CM, Winter RM (1990) The Baller-Gerold syndrome: phenotypic and cytogenetic overlap with Roberts syndrome. J Med Genet 27: 371-375
-
(1990)
J Med Genet
, vol.27
, pp. 371-375
-
-
Huson, S.M.1
Rodgers, C.S.2
Hall, C.M.3
Winter, R.M.4
-
7
-
-
0025342695
-
Variations of cervical vertebrae after expression of a Hox-I.I transgene in mice
-
Kessel M, Balling R, Gruss P (1990) Variations of cervical vertebrae after expression of a Hox-I.I transgene in mice. Cell 61: 301-308
-
(1990)
Cell
, vol.61
, pp. 301-308
-
-
Kessel, M.1
Balling, R.2
Gruss, P.3
-
8
-
-
0027944851
-
The limb bud-part two
-
Maden M (1994) The limb bud-part two. Nature 371: 560-561
-
(1994)
Nature
, vol.371
, pp. 560-561
-
-
Maden, M.1
-
9
-
-
0026352896
-
Roberts syndrome: Phenotypic variation, cytogenetic definition and heterozygote detection
-
Maserati E, Pasquali F, Zuffardi O, Buttirta P, Cuoco C, Defant G, Gimelli G, Fraccaro M (1991) Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection. Ann Genet 34: 239-246
-
(1991)
Ann Genet
, vol.34
, pp. 239-246
-
-
Maserati, E.1
Pasquali, F.2
Zuffardi, O.3
Buttirta, P.4
Cuoco, C.5
Defant, G.6
Gimelli, G.7
Fraccaro, M.8
-
10
-
-
0023010545
-
Differential and stage-related expression in embryonic tissues of a new human homeobox gene
-
Mavilio F, Simeone A, Giampaolo A, Faiella A, Zappavigna V, Acampora D, Poiana G, Russo G, Peschle C, Boncinelli E (1986) Differential and stage-related expression in embryonic tissues of a new human homeobox gene. Nature 324: 664-668
-
(1986)
Nature
, vol.324
, pp. 664-668
-
-
Mavilio, F.1
Simeone, A.2
Giampaolo, A.3
Faiella, A.4
Zappavigna, V.5
Acampora, D.6
Poiana, G.7
Russo, G.8
Peschle, C.9
Boncinelli, E.10
-
12
-
-
0346379360
-
Two human homeobox genes, c1 and c8: Structure analysis and expression in embryonic development
-
Simeone A, Mavilio F, Acampora D, Giampaolo A, Faiella A, Zappavigna V, D'Esposito M, Pannese M, Russo G, Boncinelli E, Peschle C (1987) Two human homeobox genes, c1 and c8: structure analysis and expression in embryonic development. Proc Natl Acad Sci USA 84: 4914-4918
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 4914-4918
-
-
Simeone, A.1
Mavilio, F.2
Acampora, D.3
Giampaolo, A.4
Faiella, A.5
Zappavigna, V.6
D'Esposito, M.7
Pannese, M.8
Russo, G.9
Boncinelli, E.10
Peschle, C.11
-
13
-
-
13344251211
-
Vertebral hypersegmentation: Association with gastrointestinal atresias
-
Stevenson RE (1992) Vertebral hypersegmentation: association with gastrointestinal atresias. Proc Greenwood Genet Center 11: 10-12
-
(1992)
Proc Greenwood Genet Center
, vol.11
, pp. 10-12
-
-
Stevenson, R.E.1
-
16
-
-
0027429318
-
Roberts syndrome: A review of 100 cases and a new ratine system for severity
-
Van Den Berg DJ, Francke U (1993) Roberts syndrome: a review of 100 cases and a new ratine system for severity. Am J Med Genet 47: 1104-1123
-
(1993)
Am J Med Genet
, vol.47
, pp. 1104-1123
-
-
Van Den Berg, D.J.1
Francke, U.2
-
17
-
-
0025022620
-
Mirror polydactyly: Pathogenesis based on a morphogen gradient theory
-
Viljoen DL, Kidson SH (1990) Mirror polydactyly: pathogenesis based on a morphogen gradient theory. Am J Med Genet 35: 229-235
-
(1990)
Am J Med Genet
, vol.35
, pp. 229-235
-
-
Viljoen, D.L.1
Kidson, S.H.2
-
18
-
-
8944252917
-
Relevance of the genetics of embryologic development
-
Wilson GN (1993) Relevance of the genetics of embryologic development. Growth Genet Horm 9/4: 1-5
-
(1993)
Growth Genet Horm
, vol.9
, Issue.4
, pp. 1-5
-
-
Wilson, G.N.1
|