Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype

Lignende værker

• Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH
  af: Bittel, D.C., et al.
  Udgivet: (2009)
• Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes
  af: Delio, Maria, et al.
  Udgivet: (2013)
• Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes
  af: Delio, Maria, et al.
  Udgivet: (2013)
• Deletions and duplications of the 22q11.2 region in spermatozoa from DiGeorge/velocardiofacial fathers
  af: Vergés, Laia, et al.
  Udgivet: (2014)
• In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
  af: Motahari, Zahra, et al.
  Udgivet: (2019)