共 83 条
[11]
Bachinsky DR(2001)DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1 Nat Genet 27 286-91
[12]
Lin RC(2001)TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome Cell 104 619-29
[13]
Schott JJ(2001)Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice Nature 410 97-101
[14]
Benson DW(2001)Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome Nat Genet 27 293-8
[15]
Basson CT(2002)CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle Am J Hum Genet 70 776-80
[16]
Morris CA(2000)The EGF-CFC gene family in vertebrate development Trends Genet 16 303-9
[17]
Loker J(2000)Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus Nat Genet 25 42-6
[18]
Ensing G(2002)Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis Genomics 79 475-8
[19]
Stock AD(2000)Co-localization, heterophilic interactions and regulated expression of IgLON family proteins in the chick nervous system Mol Brain Res 82 84- 94
[20]
Oda T(1996)Association of a mosaic chromosomal 22q11 deletion with hypoplastic left heart syndrome Am J Cardiol 77 1023-5