Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2 (original) (raw)

143

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Hodgson S. V., Neville B., Jones R. W., Fear C., Bobrow M. Two cases of X/autosome translocation in females with incontinentia pigmenti. Hum Genet. 1985;71(3):231–234. doi: 10.1007/BF00284581. [DOI] [PubMed] [Google Scholar]
  2. Hoo J. J. Clinical consequence of Xp-. Hum Genet. 1979 Feb 15;46(3):349–351. doi: 10.1007/BF00273321. [DOI] [PubMed] [Google Scholar]
  3. Sefiani A., Abel L., Heuertz S., Sinnett D., Lavergne L., Labuda D., Hors-Cayla M. C. The gene for incontinentia pigmenti is assigned to Xq28. Genomics. 1989 Apr;4(3):427–429. doi: 10.1016/0888-7543(89)90350-9. [DOI] [PubMed] [Google Scholar]
  4. al-Gazali L. I., Mueller R. F., Caine A., Antoniou A., McCartney A., Fitchett M., Dennis N. R. Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3. J Med Genet. 1990 Jan;27(1):59–63. doi: 10.1136/jmg.27.1.59. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. al-Gazali L. I., Mueller R. F., Caine A., Antoniou A., McCartney A., Fitchett M., Dennis N. R. Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3. J Med Genet. 1990 Jan;27(1):59–63. doi: 10.1136/jmg.27.1.59. [DOI] [PMC free article] [PubMed] [Google Scholar]