| P2093 | author name string | Nobuyoshi Shimizu | |
| | Setsuko Noda | |
| | Shinsei Minoshima | |
| | Takashi Sasaki | |
| | Aiko Shiohama | |
| P2860 | cites work | A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects | Q22008774 |
| | Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome. | Q24540203 |
| | A conserved double-stranded RNA-binding domain | Q24563195 |
| | The DNA sequence of human chromosome 22 | Q28139873 |
| | Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice | Q28204189 |
| | DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1 | Q28204282 |
| | Characterization of a novel protein-binding module--the WW domain | Q28295526 |
| | Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome | Q28505391 |
| | A new concept of the cellular basis of immunity | Q30054745 |
| | Minor-groove recognition of double-stranded RNA by the double-stranded RNA-binding domain from the RNA-activated protein kinase PKR. | Q30468875 |
| | Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome | Q33503638 |
| | DiGeorge syndrome: part of CATCH 22. | Q33595892 |
| | Prevalence of 22q11 microdeletion | Q33677732 |
| | Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study | Q33679532 |
| | NeW wrinkles for an old domain | Q34132908 |
| | Velo‐cardio‐facial syndrome: Frequency and extent of 22q1l deletions | Q34305522 |
| | A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11. | Q34394188 |
| | A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart. | Q34395108 |
| | Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients | Q35249478 |
| | Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization. | Q39410686 |
| | Automated detection of point mutations using fluorescent sequence trace subtraction | Q39724486 |
| | Velo-cardio-facial syndrome: a review of 120 patients. | Q40876751 |
| | Towards prediction of cognate complexes between the WW domain and proline-rich ligands | Q41106296 |
| | Mouse myocilin (Myoc) gene expression in ocular tissues | Q42681473 |
| | HIRA, a DiGeorge syndrome candidate gene, is required for cardiac outflow tract septation. | Q52179821 |
| | High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions. | Q52901694 |
| | Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome | Q61498132 |
| | Late‐Onset psychosis in the velo‐cardio‐facial syndrome | Q67484968 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | DiGeorge syndrome | Q525642 |
| P304 | page(s) | 184-90 | |
| P577 | publication date | 2003-04-25 | |
| P1433 | published in | Biochemical and Biophysical Research Communications | Q864228 |
| P1476 | title | Molecular cloning and expression analysis of a novel gene DGCR8 located in the DiGeorge syndrome chromosomal region | |
| P478 | volume | 304 | |