Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly

Antzeko izenburuak

• Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome
  nork: Yatsenko, Svetlana A., et al.
  Argitaratua: (2009)
• Trigonocephaly and the Opitz C syndrome.
  nork: Sargent, C, et al.
  Argitaratua: (1985)
• Phenotype and variations associated with the deletion of the 1q44 cytoband and the pathogenic duplication in the 9q32q34.3 cytobands
  nork: Gómez-Carpintero García, Ana, et al.
  Argitaratua: (2020)
• A report of a child with a deletion (9)(q34.3): a recognisable phenotype?
  nork: Ayyash, H, et al.
  Argitaratua: (1997)
• Novel 9q34.11 gene deletions encompassing combinations of four Mendelian disease genes: STXBP1, SPTAN1, ENG, and TOR1A
  nork: Campbell, Ian M., et al.
  Argitaratua: (2012)