Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2.
Open Access
- 1 February 1991
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 28 (2) , 143-144
- https://doi.org/10.1136/jmg.28.2.143-a
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Cornelia de Lange syndrome with ring chromosome 3.Journal of Medical Genetics, 1990
- Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.Journal of Medical Genetics, 1990
- The gene for incontinentia pigmenti is assigned to Xq28Genomics, 1989
- Two cases of X/autosome translocation in females with incontinentia pigmentiHuman Genetics, 1985
- Chromosome 3q duplicationand the brachmann-de lange syndrome (BDLS)The Journal of Pediatrics, 1979
- Clinical consequence of Xp-Human Genetics, 1979
- The association of chromosome 3 duplication and the Correlia de Lange syndromeThe Journal of Pediatrics, 1978