Is the genetic basis of DiGeorge syndrome in HAND?

[1] DEPENDENCE OF THYMUS DEVELOPMENT ON DERIVATIVES OF THE NEURAL CREST [J]. SCIENCE, 1984, 223 (4635) : 498 - 500

[2] CLONING A BALANCED TRANSLOCATION ASSOCIATED WITH DIGEORGE-SYNDROME AND IDENTIFICATION OF A DISRUPTED CANDIDATE GENE [J]. NATURE GENETICS, 1995, 10 (03) : 269 - 278

[3] DiGeorge AM, 1968, BIRTH DEFECTS OAS, VIV, P116

[4] Mutation of the angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation [J]. NEURON, 1998, 21 (04) : 799 - 811

[5] A PROTEOLYTIC PATHWAY THAT RECOGNIZES UBIQUITIN AS A DEGRADATION SIGNAL [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (29) : 17442 - 17456

[6] UBE3A/E6-AP mutations cause Angelman syndrome [J]. NATURE GENETICS, 1997, 15 (01) : 70 - 73

[7] Congenital heart defects and 22q11 deletions: which genes count? [J]. MOLECULAR MEDICINE TODAY, 1998, 4 (08): : 350 - 357

[8] De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome [J]. NATURE GENETICS, 1997, 15 (01) : 74 - 77

[9] Direct selection of conserved cDNAs from the DiGeorge critical region: Isolation of a novel CDC45-like gene [J]. GENOME RESEARCH, 1998, 8 (08) : 834 - 841

[10] UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome [J]. HUMAN MOLECULAR GENETICS, 1997, 6 (02) : 259 - 265

[1] DEPENDENCE OF THYMUS DEVELOPMENT ON DERIVATIVES OF THE NEURAL CREST [J]. SCIENCE, 1984, 223 (4635) : 498 - 500

[2] CLONING A BALANCED TRANSLOCATION ASSOCIATED WITH DIGEORGE-SYNDROME AND IDENTIFICATION OF A DISRUPTED CANDIDATE GENE [J]. NATURE GENETICS, 1995, 10 (03) : 269 - 278

[3] DiGeorge AM, 1968, BIRTH DEFECTS OAS, VIV, P116

[4] Mutation of the angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation [J]. NEURON, 1998, 21 (04) : 799 - 811

[5] A PROTEOLYTIC PATHWAY THAT RECOGNIZES UBIQUITIN AS A DEGRADATION SIGNAL [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (29) : 17442 - 17456

[6] UBE3A/E6-AP mutations cause Angelman syndrome [J]. NATURE GENETICS, 1997, 15 (01) : 70 - 73

[7] Congenital heart defects and 22q11 deletions: which genes count? [J]. MOLECULAR MEDICINE TODAY, 1998, 4 (08): : 350 - 357

[8] De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome [J]. NATURE GENETICS, 1997, 15 (01) : 74 - 77

[9] Direct selection of conserved cDNAs from the DiGeorge critical region: Isolation of a novel CDC45-like gene [J]. GENOME RESEARCH, 1998, 8 (08) : 834 - 841

[10] UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome [J]. HUMAN MOLECULAR GENETICS, 1997, 6 (02) : 259 - 265