-
1
-
-
0026750771
-
A genetic etiology for DiGeorge syndrome: Consistent deletions and microdeletions of 22q11
-
Driscoll,D.A., Budarf,M.L. and Emanuel,B.S. (1992) A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11. Am. J. Hum. Genet., 50, 924-933.
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 924-933
-
-
Driscoll, D.A.1
Budarf, M.L.2
Emanuel, B.S.3
-
2
-
-
0026662962
-
Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome
-
Driscoll,D.A., Spinner,N.B., Budarf,M.L., McDonald-McGinn,D.M., Zackai,E.H., Goldberg,R.B., Shprintzen,R.J., Saal,H.M., Zonana,J., Jones,M.C. and Emanuel,B.S. (1992) Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome. Am. J. Med. Genet., 44, 261-268.
-
(1992)
Am. J. Med. Genet.
, vol.44
, pp. 261-268
-
-
Driscoll, D.A.1
Spinner, N.B.2
Budarf, M.L.3
McDonald-McGinn, D.M.4
Zackai, E.H.5
Goldberg, R.B.6
Shprintzen, R.J.7
Saal, H.M.8
Zonana, J.9
Jones, M.C.10
Emanuel, B.S.11
-
3
-
-
0000690417
-
-
Rimoin,D.L., Connor,J.M. and Pyeritz,R.E. (eds), Churchill Livingstone, New York, NY
-
Bum,J. and Goodship,J. (1996) In Rimoin,D.L., Connor,J.M. and Pyeritz,R.E. (eds), Embery and Rimoin's Principles and Practice of Medical Genetics. Churchill Livingstone, New York, NY, pp. 767-828.
-
(1996)
Embery and Rimoin's Principles and Practice of Medical Genetics
, pp. 767-828
-
-
Bum, J.1
Goodship, J.2
-
4
-
-
0027400375
-
Velo-cardio-facial syndrome: A review of 120 patients
-
Goldberg,R., Motzkin,B., Marion,R., Scambler,P.J. and Shprintzen,R.J. (1993) Velo-cardio-facial syndrome: a review of 120 patients. Am. J. Med. Genet., 45, 313-319.
-
(1993)
Am. J. Med. Genet.
, vol.45
, pp. 313-319
-
-
Goldberg, R.1
Motzkin, B.2
Marion, R.3
Scambler, P.J.4
Shprintzen, R.J.5
-
5
-
-
0031132215
-
Chromosomes 22q11 deletion syndrome: An update and review for the primary pediatrician
-
Thomas,J.A. and Graham,J.,Jr (1997) Chromosomes 22q11 deletion syndrome: an update and review for the primary pediatrician. Clin. Pediat., 36, 253-266.
-
(1997)
Clin. Pediat.
, vol.36
, pp. 253-266
-
-
Thomas, J.A.1
Graham Jr., J.2
-
6
-
-
0027296236
-
Variable phenotypes in Velo-cardio-facial syndrome with chromosomal deletion
-
Motzkin,B., Marion,R., Goldberg,R., Shprintzen,R. and Saenger,P. (1993) Variable phenotypes in Velo-cardio-facial syndrome with chromosomal deletion. J. Pediat., 123, 406-410.
-
(1993)
J. Pediat.
, vol.123
, pp. 406-410
-
-
Motzkin, B.1
Marion, R.2
Goldberg, R.3
Shprintzen, R.4
Saenger, P.5
-
7
-
-
0029853761
-
Bipolar spectrum disorders in patients diagnosed with Velo-cardio-facial syndrome: Does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
-
Papolos,D.F., Faedda,G.L., Veit,S., Goldberg,R., Morrow,B., Kucherlapati,R. and Shprintzen,R.J. (1996) Bipolar spectrum disorders in patients diagnosed with Velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder? Am. J. Psychiat., 153, 1541-1547.
-
(1996)
Am. J. Psychiat.
, vol.153
, pp. 1541-1547
-
-
Papolos, D.F.1
Faedda, G.L.2
Veit, S.3
Goldberg, R.4
Morrow, B.5
Kucherlapati, R.6
Shprintzen, R.J.7
-
8
-
-
0030910606
-
Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders
-
Carlson,C., Papolos,D., Pandita,R.K., Faedda,G.L., Veit,S., Goldberg,R., Shprintzen,R., Kucherlapati,R. and Morrow,B. (1997) Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders. Am. J. Hum. Genet., 60, 851-859.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 851-859
-
-
Carlson, C.1
Papolos, D.2
Pandita, R.K.3
Faedda, G.L.4
Veit, S.5
Goldberg, R.6
Shprintzen, R.7
Kucherlapati, R.8
Morrow, B.9
-
9
-
-
0027370619
-
Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: Implications for genetic counseling and prenatal diagnosis
-
Driscoll,D.A., Salvin,J., Sellinger,B., Budarf,M.L., McDonald-McGinn,D.M., Zackai,E.H. and Emanuel,B.S. (1993) Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counseling and prenatal diagnosis. J. Med. Genet., 30, 813-817.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 813-817
-
-
Driscoll, D.A.1
Salvin, J.2
Sellinger, B.3
Budarf, M.L.4
McDonald-McGinn, D.M.5
Zackai, E.H.6
Emanuel, B.S.7
-
10
-
-
0029634412
-
Velo-cardio-facial syndrome: Frequency and extent of 22q11 deletions
-
Lindsay,E.A., Goldberg,R., Jurecic,V., Morrow,B., Carlson,C., Kucherlapati,R.S., Shprintzen,R.J. and Baldini,A. (1995) Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions. Am. J. Med. Genet., 57, 514-522.
-
(1995)
Am. J. Med. Genet.
, vol.57
, pp. 514-522
-
-
Lindsay, E.A.1
Goldberg, R.2
Jurecic, V.3
Morrow, B.4
Carlson, C.5
Kucherlapati, R.S.6
Shprintzen, R.J.7
Baldini, A.8
-
11
-
-
0029033626
-
Molecular definition of the 22q11 deletions in Velo-cardio-facial syndrome
-
Morrow,B., Goldberg,R., Carlson,C., Das Gupta,R., Sirotkin,H., Collins,J., Dunham,I., O'Donnell,H., Scambler,P., Shprintzen,R. and Kucherlapati,R. (1995) Molecular definition of the 22q11 deletions in Velo-cardio-facial syndrome. Am. J. Hum. Genet., 56, 1391-1403.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 1391-1403
-
-
Morrow, B.1
Goldberg, R.2
Carlson, C.3
Das Gupta, R.4
Sirotkin, H.5
Collins, J.6
Dunham, I.7
O'Donnell, H.8
Scambler, P.9
Shprintzen, R.10
Kucherlapati, R.11
-
12
-
-
16944364251
-
Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients
-
Carlson,C., Sirotkin,H., Pandita,R., Goldberg,R., McKie,J., Wadey,R., Patanjali,S.R., Weissman,S.M., Anyane-Yeboa,K., Warburton,D., Scambler,P., Shprintzen,R., Kucherlapati,R. and Morrow,B.E. (1997) Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients. Am. J. Hum. Genet., 61, 620-629.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 620-629
-
-
Carlson, C.1
Sirotkin, H.2
Pandita, R.3
Goldberg, R.4
McKie, J.5
Wadey, R.6
Patanjali, S.R.7
Weissman, S.M.8
Anyane-Yeboa, K.9
Warburton, D.10
Scambler, P.11
Shprintzen, R.12
Kucherlapati, R.13
Morrow, B.E.14
-
13
-
-
0029938855
-
How many breaks do we need to CATCH on 22q11?
-
Dallapiccola,B., Pizzuti,A. and Novelli,G. (1996) How many breaks do we need to CATCH on 22q11?. Am. J. Hum. Genet., 59, 7-11.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 7-11
-
-
Dallapiccola, B.1
Pizzuti, A.2
Novelli, G.3
-
14
-
-
0030756674
-
Progress in the autosomal segmental aneusomy syndromes (SASs): Single or multi-locus disorders?
-
Budarf,M.L. and Emanuel,B.S. (1997) Progress in the autosomal segmental aneusomy syndromes (SASs): single or multi-locus disorders? Hum. Mol. Genet., 6, 1657-1665.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1657-1665
-
-
Budarf, M.L.1
Emanuel, B.S.2
-
15
-
-
0030588069
-
Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3
-
Brown,J., Dry,K.L., Edgar,A.J., Pryde,F.E., Hardwick,L.J., Aldred,M.A., Lester,D.H., Boyle,S., Kaplan,J., Dufier,J.L., Ho,M.F., Monaco,A.M., Musarella,M.A. and Wright,A.F. (1996) Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3. Genomics, 37, 200-210.
-
(1996)
Genomics
, vol.37
, pp. 200-210
-
-
Brown, J.1
Dry, K.L.2
Edgar, A.J.3
Pryde, F.E.4
Hardwick, L.J.5
Aldred, M.A.6
Lester, D.H.7
Boyle, S.8
Kaplan, J.9
Dufier, J.L.10
Ho, M.F.11
Monaco, A.M.12
Musarella, M.A.13
Wright, A.F.14
-
16
-
-
0030042376
-
FISH studies in a patient with sporadic aniridia and t(7;11) (q31.2;p13)
-
Crolla,J.A., Cross,I., Atkey,N., Wright,M. and Oley,C.A. (1996) FISH studies in a patient with sporadic aniridia and t(7;11) (q31.2;p13). J. Med. Genet., 33, 66-68.
-
(1996)
J. Med. Genet.
, vol.33
, pp. 66-68
-
-
Crolla, J.A.1
Cross, I.2
Atkey, N.3
Wright, M.4
Oley, C.A.5
-
17
-
-
0030057538
-
Translocation breakpoints in three patients with Campomelic Dysphasia and autosomal sex reversal map more than 130 kb from SOX9
-
Wirth,J., Wagner,T., Meyer,J., Pfeiffer,R.A., Tietze,H.U., Schempp,W. and Scherer,G. (1996) Translocation breakpoints in three patients with Campomelic Dysphasia and autosomal sex reversal map more than 130 kb from SOX9.Hum.Genet.,97, 186-193.
-
(1996)
Hum.Genet.
, vol.97
, pp. 186-193
-
-
Wirth, J.1
Wagner, T.2
Meyer, J.3
Pfeiffer, R.A.4
Tietze, H.U.5
Schempp, W.6
Scherer, G.7
-
18
-
-
0029975533
-
Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome
-
Sutherland,H.F., Wadey,R., McKie,J.M., Taylor,C., Atif,U., Johnstone,K.A., Halford,S., Kim,U.J., Goodship,J., Baldini,A. and Scambler,P.J. (1996) Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome. Am. J. Hum. Genet., 59, 23-31.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 23-31
-
-
Sutherland, H.F.1
Wadey, R.2
McKie, J.M.3
Taylor, C.4
Atif, U.5
Johnstone, K.A.6
Halford, S.7
Kim, U.J.8
Goodship, J.9
Baldini, A.10
Scambler, P.J.11
-
19
-
-
0004007167
-
-
Cambridge University Press, Cambridge, UK
-
Le Douarin,N. (1980) The Neural Crest. Cambridge University Press, Cambridge, UK.
-
(1980)
The Neural Crest
-
-
Le Douarin, N.1
-
20
-
-
0027438076
-
Patterning of neural crest derivatives in the avian embryo: In vivo and in vitro studies
-
Le Douarin,N.M., Ziller,C. and Couly,G.F. (1993) Patterning of neural crest derivatives in the avian embryo: in vivo and in vitro studies. Dev. Biol., 159, 24-49.
-
(1993)
Dev. Biol.
, vol.159
, pp. 24-49
-
-
Le Douarin, N.M.1
Ziller, C.2
Couly, G.F.3
-
21
-
-
0029142767
-
Neural crest and cardiovascular patterning
-
Kirby,M.L. and Waldo,K.L. (1995) Neural crest and cardiovascular patterning. Circulation Res., 77, 211-215.
-
(1995)
Circulation Res.
, vol.77
, pp. 211-215
-
-
Kirby, M.L.1
Waldo, K.L.2
-
22
-
-
0030747208
-
Homeobox genes in embryogenesis and pathogenesis
-
Mark,M., Rijli,F.M. and Chambon,P. (1997) Homeobox genes in embryogenesis and pathogenesis. Pediat. Res., 42, 421-429.
-
(1997)
Pediat. Res.
, vol.42
, pp. 421-429
-
-
Mark, M.1
Rijli, F.M.2
Chambon, P.3
-
23
-
-
0030879040
-
Homeobox genes and disease
-
Boncinelli,E. (1997) Homeobox genes and disease. Curr. Opin. Genet. Dev., 7, 331-337.
-
(1997)
Curr. Opin. Genet. Dev.
, vol.7
, pp. 331-337
-
-
Boncinelli, E.1
-
24
-
-
0031436593
-
Role of HOX genes in human development
-
Innis,J.W. (1997) Role of HOX genes in human development. Curr. Opin. Pediat., 9, 617-622.
-
(1997)
Curr. Opin. Pediat.
, vol.9
, pp. 617-622
-
-
Innis, J.W.1
-
25
-
-
0031170969
-
Genetic analysis of craniofacial development in the vertebrate embryo
-
Schilling,T.F. (1997) Genetic analysis of craniofacial development in the vertebrate embryo. Bioessays, 19, 459-468.
-
(1997)
Bioessays
, vol.19
, pp. 459-468
-
-
Schilling, T.F.1
-
26
-
-
0025797513
-
Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5
-
Chisaka,O. and Capecchi,M.R. (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
-
27
-
-
0029124998
-
Goosecoid is not an essential component of the mouse gastrula organizer but is required for craniofacial and rib development
-
Rivera-Perez,J.A., Mallo,M., Gendron-Maguire,M., Gridley,T. and Behringer,R.R. (1995) Goosecoid is not an essential component of the mouse gastrula organizer but is required for craniofacial and rib development. Development, 121, 3005-3012.
-
(1995)
Development
, vol.121
, pp. 3005-3012
-
-
Rivera-Perez, J.A.1
Mallo, M.2
Gendron-Maguire, M.3
Gridley, T.4
Behringer, R.R.5
-
28
-
-
0029082929
-
Targeted mutation of the murine goosecoid gene results in craniofacial defects and neonatal death
-
Yamada,G., Mansouri,A., Torres,M., Stuart,E.T., Blum,M., Schullz,M., De Robertis,E.M. and Gruss,P. (1995) Targeted mutation of the murine goosecoid gene results in craniofacial defects and neonatal death. Development, 121, 2917-2922.
-
(1995)
Development
, vol.121
, pp. 2917-2922
-
-
Yamada, G.1
Mansouri, A.2
Torres, M.3
Stuart, E.T.4
Blum, M.5
Schullz, M.6
De Robertis, E.M.7
Gruss, P.8
-
29
-
-
0031040876
-
Pax3 is required for cardiac neural crest migration in the mouse: Evidence from the splotch (Sp2H) mutant
-
Conway,S.J., Henderson,D.J. and Copp,A.J. (1997) Pax3 is required for cardiac neural crest migration in the mouse: evidence from the splotch (Sp2H) mutant. Development, 124, 505-514.
-
(1997)
Development
, vol.124
, pp. 505-514
-
-
Conway, S.J.1
Henderson, D.J.2
Copp, A.J.3
-
30
-
-
0031573850
-
Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11
-
Funke,B., Saint-Jore,B., Puech,A., Sirotkin,H., Edelmann,L., Carlson,C., Raft,S., Pandita,R.K., Kucherlapati,R., Skoultchi,A. and Morrow,B.E. (1997) Characterization and mutation analysis of goosecoid-like (GSCL), a homeodomain-containing gene that maps to the critical region for VCFS/DGS on 22q11. Genomics, 46, 364-372.
-
(1997)
Genomics
, vol.46
, pp. 364-372
-
-
Funke, B.1
Saint-Jore, B.2
Puech, A.3
Sirotkin, H.4
Edelmann, L.5
Carlson, C.6
Raft, S.7
Pandita, R.K.8
Kucherlapati, R.9
Skoultchi, A.10
Morrow, B.E.11
-
31
-
-
0030940093
-
The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development
-
Gottlieb,S., Emanuel,B.S., Driscoll,D.A., Sellinger,B., Wang,Z., Roe,B. and Budarf,M.L. (1997) The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development. Am. J. Hum. Genet., 60, 1194-1201.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1194-1201
-
-
Gottlieb, S.1
Emanuel, B.S.2
Driscoll, D.A.3
Sellinger, B.4
Wang, Z.5
Roe, B.6
Budarf, M.L.7
-
32
-
-
0028236069
-
Molecular cloning of the human homeobox gene goosecoid (GSC) and mapping of the gene to human chromosome 14q32.1
-
Blum,M., De Robertis,E.M., Kojis,T., Heinzmann,C., Klisak,I., Geissert,D. and Sparkes,R.S. (1994) Molecular cloning of the human homeobox gene goosecoid (GSC) and mapping of the gene to human chromosome 14q32.1. Genomics, 21, 388-393.
-
(1994)
Genomics
, vol.21
, pp. 388-393
-
-
Blum, M.1
De Robertis, E.M.2
Kojis, T.3
Heinzmann, C.4
Klisak, I.5
Geissert, D.6
Sparkes, R.S.7
-
33
-
-
0026649645
-
Gastrulation in the mouse: The role of the homeobox gene goosecoid
-
Blum,M., Gaunt,S.J., Cho,K.W., Steinbeisser,H., Blumberg,B., Bittner,D. and De Robertis,E.M. (1992) Gastrulation in the mouse: the role of the homeobox gene goosecoid. Cell, 69, 1097-1106.
-
(1992)
Cell
, vol.69
, pp. 1097-1106
-
-
Blum, M.1
Gaunt, S.J.2
Cho, K.W.3
Steinbeisser, H.4
Blumberg, B.5
Bittner, D.6
De Robertis, E.M.7
-
34
-
-
0027521087
-
Expression of the mouse goosecoid gene during mid-embryogenesis may mark mesenchymal cell lineages in the developing head, limbs and body wall
-
Gaunt,S.J., Blum,M. and De Robertis,E.M. (1993) Expression of the mouse goosecoid gene during mid-embryogenesis may mark mesenchymal cell lineages in the developing head, limbs and body wall. Development, 117, 769-778.
-
(1993)
Development
, vol.117
, pp. 769-778
-
-
Gaunt, S.J.1
Blum, M.2
De Robertis, E.M.3
-
35
-
-
0031587979
-
Correlation between loss of middle ear bones and altered goosecoid gene expression in the branchial region following retinoic acid treatment of mouse embryos in vivo
-
Zhu,C.C., Yamada,G. and Blum,M. (1997) Correlation between loss of middle ear bones and altered goosecoid gene expression in the branchial region following retinoic acid treatment of mouse embryos in vivo. Biochem. Biophys. Res. Commun., 235, 748-753.
-
(1997)
Biochem. Biophys. Res. Commun.
, vol.235
, pp. 748-753
-
-
Zhu, C.C.1
Yamada, G.2
Blum, M.3
-
36
-
-
15144349175
-
A region of mouse chromosome 16 is syntenic to the DiGeorge, velo-cardiofacial syndrome minimal critical region
-
Galili,N., Baldwin,H.S., Lund,J., Reeves,R., Gong,W., Wang,Z., Roe,B.A., Emanuel,B.S., Nayak,S., Mickanin,C., Budarf,M.I. and Buck,C.A. (1997) A region of mouse chromosome 16 is syntenic to the DiGeorge, velo-cardiofacial syndrome minimal critical region. Genome Res., 7, 17-26.
-
(1997)
Genome Res.
, vol.7
, pp. 17-26
-
-
Galili, N.1
Baldwin, H.S.2
Lund, J.3
Reeves, R.4
Gong, W.5
Wang, Z.6
Roe, B.A.7
Emanuel, B.S.8
Nayak, S.9
Mickanin, C.10
Budarf, M.I.11
Buck, C.A.12
-
37
-
-
0029091809
-
WW6: An embryonic stem cell line with an inert genetic marker that can be traced in chimeras
-
Ioffe,E., Liu,Y., Bhaumik,M., Poirier,F., Factor,S. and Stanley,P. (1995) WW6: an embryonic stem cell line with an inert genetic marker that can be traced in chimeras. Proc. Natl Acad. Sci. USA, 92, 7357-7361.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 7357-7361
-
-
Ioffe, E.1
Liu, Y.2
Bhaumik, M.3
Poirier, F.4
Factor, S.5
Stanley, P.6
-
39
-
-
0031970423
-
Gscl, a gene within the minimal DiGeorge critical region, is expressed in primordial germ cells and the developing pons
-
Galili,N., Epstein,J.A., Leconte,I., Nayak,S. and Buck,C.A. (1998) Gscl, a gene within the minimal DiGeorge critical region, is expressed in primordial germ cells and the developing pons. Dev. Dyn., 212, 86-93.
-
(1998)
Dev. Dyn.
, vol.212
, pp. 86-93
-
-
Galili, N.1
Epstein, J.A.2
Leconte, I.3
Nayak, S.4
Buck, C.A.5
-
40
-
-
0024539502
-
Evaluation of the effect of selective germ cell depletion on subsequent spermatogenesis and fertility in the rat
-
Ratnasooriya,W.D. and Sharpe,R.M. (1989) Evaluation of the effect of selective germ cell depletion on subsequent spermatogenesis and fertility in the rat. Int. J. Androl., 12, 44-57.
-
(1989)
Int. J. Androl.
, vol.12
, pp. 44-57
-
-
Ratnasooriya, W.D.1
Sharpe, R.M.2
-
41
-
-
0344624854
-
Goosecoid and Goosecoid-related genes in mouse embryogenesis
-
Wakamiya,M., Riviera-Perez,J.A., Baldini,A. and Behringer,R.R. (1997) Goosecoid and Goosecoid-related genes in mouse embryogenesis. Cold Spring Harbor Symp. Quant. Biol., 62, 145-149.
-
(1997)
Cold Spring Harbor Symp. Quant. Biol.
, vol.62
, pp. 145-149
-
-
Wakamiya, M.1
Riviera-Perez, J.A.2
Baldini, A.3
Behringer, R.R.4
-
42
-
-
0030610994
-
Goosecoid and HNF-3β genetically interact to regulate neural tube patterning during mouse embryogenesis
-
Filosa,S., Rivera-Perez,J.A., Gomez,A.P., Gansmuller,A., Sasaki,H., Behringer,R.R. and Ang,S.L. (1997) Goosecoid and HNF-3β genetically interact to regulate neural tube patterning during mouse embryogenesis. Development, 124, 2843-2854.
-
(1997)
Development
, vol.124
, pp. 2843-2854
-
-
Filosa, S.1
Rivera-Perez, J.A.2
Gomez, A.P.3
Gansmuller, A.4
Sasaki, H.5
Behringer, R.R.6
Ang, S.L.7
-
43
-
-
0029026227
-
The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages
-
Martin,J.F., Bradley,A. and Olson,E.N. (1995) The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages. Genes Dev., 9, 1237-1249.
-
(1995)
Genes Dev.
, vol.9
, pp. 1237-1249
-
-
Martin, J.F.1
Bradley, A.2
Olson, E.N.3
-
44
-
-
0031058266
-
The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients
-
Wilming,L.G., Snoeren,C.A., van Rijswijk,A., Grosveld,F. and Meijers,C. (1997) The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients. Hum. Mol. Genet., 6, 247-258.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 247-258
-
-
Wilming, L.G.1
Snoeren, C.A.2
Van Rijswijk, A.3
Grosveld, F.4
Meijers, C.5
-
45
-
-
0342658137
-
Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development
-
Chapman,D.L., Garvey,N., Hancock,S., Alexiou,M., Agulnik,S.I., GibsonBrown,J.J., Cebra-Thomas,J., Bollag,R.J., Silver,L.M. and Papaioannou,V.E. (1996) Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development. Dev. Dyn., 206, 379-390.
-
(1996)
Dev. Dyn.
, vol.206
, pp. 379-390
-
-
Chapman, D.L.1
Garvey, N.2
Hancock, S.3
Alexiou, M.4
Agulnik, S.I.5
GibsonBrown, J.J.6
Cebra-Thomas, J.7
Bollag, R.J.8
Silver, L.M.9
Papaioannou, V.E.10
-
46
-
-
0031215021
-
Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene
-
Chieffo,C., Garvey,N., Gong,W., Roe,B., Zhang,G., Silver,L., Emanuel,B.S. and Budarf,M.L. (1997) Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene. Genomics, 43, 267-277.
-
(1997)
Genomics
, vol.43
, pp. 267-277
-
-
Chieffo, C.1
Garvey, N.2
Gong, W.3
Roe, B.4
Zhang, G.5
Silver, L.6
Emanuel, B.S.7
Budarf, M.L.8
-
47
-
-
0031924599
-
ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene
-
Lindsay,E.A., Harvey,E.L., Scambler,P.J. and Baldini,A. (1998) ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene. Hum Mol. Genet., 7, 629-635.
-
(1998)
Hum Mol. Genet.
, vol.7
, pp. 629-635
-
-
Lindsay, E.A.1
Harvey, E.L.2
Scambler, P.J.3
Baldini, A.4
-
48
-
-
0029745410
-
Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome
-
Lachman,H.M., Morrow,B., Shprintzen,R., Veit,S., Parsia,S.S., Faedda,G., Goldberg,R., Kucherlapati,R. and Papolos,D.F. (1996) Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome. Am. J. Med. Genet., 67, 468-472.
-
(1996)
Am. J. Med. Genet.
, vol.67
, pp. 468-472
-
-
Lachman, H.M.1
Morrow, B.2
Shprintzen, R.3
Veit, S.4
Parsia, S.S.5
Faedda, G.6
Goldberg, R.7
Kucherlapati, R.8
Papolos, D.F.9
-
49
-
-
0029562967
-
Chromosome engineering in mice
-
Ramirez-Solis,R., Liu,P. and Bradley,A. (1995) Chromosome engineering in mice. Nature, 378, 720-724.
-
(1995)
Nature
, vol.378
, pp. 720-724
-
-
Ramirez-Solis, R.1
Liu, P.2
Bradley, A.3
-
50
-
-
0026521157
-
A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers
-
Hazan,J., Dubay,C., Pankowiak,M.P., Becuwe,N. and Weissenbach,J. (1992) A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers. Genomics, 12, 183-189.
-
(1992)
Genomics
, vol.12
, pp. 183-189
-
-
Hazan, J.1
Dubay, C.2
Pankowiak, M.P.3
Becuwe, N.4
Weissenbach, J.5
-
52
-
-
0004136246
-
-
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Sambrook,J., Fritsch,E.F. and Maniatis,T. (1989) Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
53
-
-
0025739379
-
Simplified mammalian DNA isolation procedure
-
Laird,P.W., Zijderveld,A., Linders,K., Rudnicki,M.A., Jaenisch,R. and Bems,A. (1991) Simplified mammalian DNA isolation procedure. Nucleic Acids Res., 19, 4293.
-
(1991)
Nucleic Acids Res.
, vol.19
, pp. 4293
-
-
Laird, P.W.1
Zijderveld, A.2
Linders, K.3
Rudnicki, M.A.4
Jaenisch, R.5
Bems, A.6
-
56
-
-
0021838285
-
Construction of a fusion gene that confers resistance against hygromycin B to mammalian cells in culture
-
Bernard,H.U., Krammer,G. and Rowekamp,W.G. (1985) Construction of a fusion gene that confers resistance against hygromycin B to mammalian cells in culture. Exp. Cell Res., 158, 237-243.
-
(1985)
Exp. Cell Res.
, vol.158
, pp. 237-243
-
-
Bernard, H.U.1
Krammer, G.2
Rowekamp, W.G.3
-
57
-
-
0023945548
-
Efficient transformation of mammalian cells with constructs containing a puromycin-resistance marker
-
de la Luna,S., Soria,I., Pulido,D., Ortin,J. and Jimenez,A. (1988) Efficient transformation of mammalian cells with constructs containing a puromycin-resistance marker. Gene, 62, 121-126.
-
(1988)
Gene
, vol.62
, pp. 121-126
-
-
De La Luna, S.1
Soria, I.2
Pulido, D.3
Ortin, J.4
Jimenez, A.5
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