I Cross

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

John Burn, Atsuyoshi Takao, David I. Wilson et al. · Journal of Medical Genetics · 1993 · 269 citations · Full text

Probe Do832, Developmental Anomaly, Genetic Disorder +11

A population study of chromosome 22q11 deletions in infancy

Judith Goodship, I Cross, Jesse Li‐Ling et al. · Archives of Disease in Childhood · 1998 · 250 citations · Full text

Confirmation that the velo‐cardio‐facial syndrome is associated with haplo‐insufficiency of genes at chromosome 22q11

David A. Kelly, Rosalie Goldberg, David I. Wilson et al. · American Journal of Medical Genetics · 1993 · 181 citations

Down Syndrome, Velo‐cardio‐facial Syndrome, Developmental Biology +15

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

Stephanle Halford, Roy Wadey, Catherine Roberts et al. · Human Molecular Genetics · 1993 · 140 citations

Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.

Judith Goodship, I Cross, Peter Scambler et al. · Journal of Medical Genetics · 1995 · 134 citations · Full text

Developmental Anomaly, Chromosome Dynamics, Developmental Biology +14