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

Ítems similars

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