Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
January 1, 1996Mental Retardation and Developmental Disabilities Research ReviewsOpen Access

DiGeorge and velocardiofacial syndromes: The 22q11 deletion syndrome

View Full Paper
Ask AI
Bookmark
Share

Authors

DDDeborah A. DriscollRutgers, The State University of New JerseyBEBeverly S. EmanuelChildren's Hospital of Philadelphia

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Driscoll et al. (1996) studied this question.

synapsesocial.com/papers/6a92f176cfcd15eebf77203dhttps://doi.org/10.1002/(sici)1098-2779(1996)2:3<130::aid-mrdd3>3.0.co;2-w
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.1993 · 490 citations
  2. 2Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease1993 · 141 citations
  3. 3Genomic scan for genes predisposing to schizophrenia1994 · 167 citations
  4. 4Isolation and characterization of a novel gene deleted in DiGeorge syndrome1995 · 72 citations
  5. 5DiGeorge anomaly with renal agenesis in infants of mothers with diabetes1993 · 66 citations