Author:
Debrus S.,Berger G.,de Meeus A.,Sauer U.,Guillaumont S.,Voisin M.,Bozio A.,Demczuk S.,Aurias A.,Bouvagnet P.
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference27 articles.
1. Amati F, Mari A, Digilio MC, Mingarelli R, Giannotti A, Novelli G, Dallapiccola B (1995) 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot. Hum Genet 95:479–482
2. Aubry M, Demczuk S, Desmaze C, Aikem M, Aurias A, Julien JP, Rouleau GA (1993) Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome. Hum Mol Genet 2:1583–1587
3. Burn J, Takao A, Wilson D, Cross I, Momma K, Wadey R, Scambler P, Goodship J (1993) Conotruncal anomaly face syndrome face syndrome is associated with a deletion within chromosomes 22q11. J Med Genet 30:822–824
4. Carey AH, Kelly D, Halford S, Wadey R, Wilson D, Goodship J, Burn J, Paul T, Sharkey A, Dumanski J, Nordenskjold M, Williamson R, Scambler PJ (1992) Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome. Am J Hum Genet 51:964–970
5. Demczuk S, Levy A, Aubry M, Croquette MF, Philip N, Prieur M, Sauer U, Bouvagnet P, Rouleau GA, Thomas G, Aurias A (1995) Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature. Hum Genet 96:9–13
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