22q11 deletion syndrome (Q18554351)

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chromosomal disease that has material basis in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features
  • Shprintzen syndrome
  • VCF-Velocardiofacial syndrome
  • deletion 22q11.2 syndrome
  • velocardiofacial syndrome
  • VCFS
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English
22q11 deletion syndrome
chromosomal disease that has material basis in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features
  • Shprintzen syndrome
  • VCF-Velocardiofacial syndrome
  • deletion 22q11.2 syndrome
  • velocardiofacial syndrome
  • VCFS

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