-
1
-
-
0022868252
-
DiGeorge syndrome and 22q11 rearrangements
-
Augusseau, S., S. Jouk, P. Jalbert, and M. Prieur. 1986. DiGeorge syndrome and 22q11 rearrangements. Hum. Genet. 74: 206.
-
(1986)
Hum. Genet.
, vol.74
, pp. 206
-
-
Augusseau, S.1
Jouk, S.2
Jalbert, P.3
Prieur, M.4
-
2
-
-
84941143640
-
Shotgun cloning as the strategy of choice to generate templates for high throughput dideoxynucleotide sequencing
-
ed. M.D. Adams, C. Fields, and C. Venter, Academic Press, London, UK
-
Bodenteich, A., S.L. Chissoe, Y.F. Wang, and B.A. Roe. 1994. Shotgun cloning as the strategy of choice to generate templates for high throughput dideoxynucleotide sequencing. In Automated DNA sequencing and analysis techniques (ed. M.D. Adams, C. Fields, and C. Venter), pp. 42-50. Academic Press, London, UK.
-
(1994)
Automated DNA Sequencing and Analysis Techniques
, pp. 42-50
-
-
Bodenteich, A.1
Chissoe, S.L.2
Wang, Y.F.3
Roe, B.A.4
-
3
-
-
0028998317
-
Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene
-
Budarf, M.L., J. Collins, W. Gong, B. Roe, Z. Wang, L.C. Bailey, B. Sellinger, D. Michaud, D.A. Driscoll, and B.S. Emanuel. 1995. Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene. Nature Genet. 10: 269-278.
-
(1995)
Nature Genet.
, vol.10
, pp. 269-278
-
-
Budarf, M.L.1
Collins, J.2
Gong, W.3
Roe, B.4
Wang, Z.5
Bailey, L.C.6
Sellinger, B.7
Michaud, D.8
Driscoll, D.A.9
Emanuel, B.S.10
-
4
-
-
0027373693
-
Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11
-
Burn, J., A. Takao, D. Wilson, I. Cross, K. Momma, R. Wadey, P. Scambler, and J. Goodship. 1993. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11. J. Med. Genet. 30: 822-824.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 822-824
-
-
Burn, J.1
Takao, A.2
Wilson, D.3
Cross, I.4
Momma, K.5
Wadey, R.6
Scambler, P.7
Goodship, J.8
-
5
-
-
0025080192
-
Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome
-
Carey, A.H., S. Roach, R. Williamson, J.P. Dumanski, M. Nordenskjöld, V.P. Collins, G.A. Rouleau, N. Blin, P. Jalbert, and P.J. Scambler. 1990. Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome. Genomics 7: 299-306.
-
(1990)
Genomics
, vol.7
, pp. 299-306
-
-
Carey, A.H.1
Roach, S.2
Williamson, R.3
Dumanski, J.P.4
Nordenskjöld, M.5
Collins, V.P.6
Rouleau, G.A.7
Blin, N.8
Jalbert, P.9
Scambler, P.J.10
-
6
-
-
0026688328
-
Molecular genetic study of the frequency of monosomy 22q11 in Digeorge syndrome
-
Carey, A.H., D. Kelly, S. Halford, R. Wadey, D. Wilson, J. Goodship, J. Burn, T. Paul, A.M. Sharkey, J.P. Dumanski, M. Nordenskjöld, R. Williamson, and P.J. Scambler. 1992. Molecular genetic study of the frequency of monosomy 22q11 in Digeorge syndrome. Am. J. Hum. Genet. 51: 964-970.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 964-970
-
-
Carey, A.H.1
Kelly, D.2
Halford, S.3
Wadey, R.4
Wilson, D.5
Goodship, J.6
Burn, J.7
Paul, T.8
Sharkey, A.M.9
Dumanski, J.P.10
Nordenskjöld, M.11
Williamson, R.12
Scambler, P.J.13
-
7
-
-
0028958564
-
Cloning of a balanced translocation breakpoint in the Digeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity
-
Demczuk, S., R. Aledo, J. Zucman, O. Delattre, C. Desmaze, L. Dauphinot, P. Jalbert, G.A. Rouleau, G. Thomas, and A. Aurias. 1995. Cloning of a balanced translocation breakpoint in the Digeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity. Hum. Mol. Genet. 4: 551-558.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 551-558
-
-
Demczuk, S.1
Aledo, R.2
Zucman, J.3
Delattre, O.4
Desmaze, C.5
Dauphinot, L.6
Jalbert, P.7
Rouleau, G.A.8
Thomas, G.9
Aurias, A.10
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