Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2.

Ítems similars

• Familial cases of a submicroscopic Xp22.2 deletion: genotype-phenotype correlation in microphthalmia with linear skin defects syndrome
  per: Vergult, Sarah, et al.
  Publicat: (2013)
• Microphthalmia, Linear Skin Defects, Callosal Agenesis, and Cleft Palate in a Patient with Deletion at Xp22.3p22.2
  per: Vendramini-Pittoli, Siulan, et al.
  Publicat: (2020)
• Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.
  per: al-Gazali, L I, et al.
  Publicat: (1990)
• Microphthalmia with linear skin defects syndrome (MIDAS)
  per: Banganho, Denise, et al.
  Publicat: (2019)
• De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies.
  per: Temple, I K, et al.
  Publicat: (1990)