Molecular cloning and expression analysis of a novel gene DGCR8 located in the DiGeorge syndrome chromosomal region

Manipulating the mouse embryo: A laboratory manual

1986 • 4,548 citations

Manipulating the mouse embryo: A laboratory manual

1986 • 2,165 citations

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

1997 • 1,187 citations

The DNA sequence of human chromosome 22

1999 • 1,167 citations

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

2001 • 1,062 citations

Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice

2001 • 996 citations

A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome.

1978 • 593 citations

A conserved double-stranded RNA-binding domain.

1992 • 540 citations

DiGeorge syndrome: part of CATCH 22.

1993 • 510 citations

Velo‐cardio‐facial syndrome: A review of 120 patients

1993 • 430 citations

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

1992 • 420 citations

Characterization of a novel protein‐binding module — the WW domain

1995 • 365 citations

Low-Copy Repeats Mediate the Common 3-Mb Deletion in Patients with Velo-cardio-facial Syndrome

1999 • 363 citations

Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome Patients

1997 • 358 citations

A new concept of the cellular basis of immunity

1965 • 352 citations

NeW Wrinkles for an Old Domain

2000 • 349 citations

Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome

2001 • 301 citations

Two RNA-binding motifs in the double-stranded RNA-activated protein kinase, DAI.

1992 • 243 citations

Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.

1995 • 243 citations

Minor-Groove Recognition of Double-Stranded RNA by the Double-Stranded RNA-Binding Domain from the RNA-Activated Protein Kinase PKR

1996 • 222 citations

A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11

1996 • 141 citations

High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions

1998 • 131 citations

Velo‐cardio‐facial syndrome: Frequency and extent of 22q1l deletions

1995 • 126 citations

Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome

1998 • 123 citations

Towards prediction of cognate complexes between the WW domain and proline‐rich ligands

1996 • 108 citations

HIRA, a DiGeorge Syndrome Candidate Gene, Is Required for Cardiac Outflow Tract Septation

1999 • 92 citations

Deletion mapping of 22q11 in CATCH22 syndrome: Identification of a second critical region

1996 • 88 citations

Molecular Cytogenetic Characterization of the DiGeorge Syndrome Region Using Fluorescence in Situ Hybridization

1993 • 84 citations

Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome

1995 • 76 citations

Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.

1999 • 69 citations

Automated detection of point mutations using fluorescent sequence trace subtraction

1998 • 69 citations

A Transcription Map in the CATCH22 Critical Region: Identification, Mapping, and Ordering of Four Novel Transcripts Expressed in Heart

1996 • 47 citations

Mouse Myocilin (Myoc) Gene Expression in Ocular Tissues1

1998 • 44 citations