Full text
PDF
Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- 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]
- Hoo J. J. Clinical consequence of Xp-. Hum Genet. 1979 Feb 15;46(3):349–351. doi: 10.1007/BF00273321. [DOI] [PubMed] [Google Scholar]
- 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]
- 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]
- 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]