The breakpoints of the EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization
- 1 July 1993
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 44 (1) , 50
- https://doi.org/10.1111/j.1399-0004.1993.tb03843.x
Abstract
Clin Genet 1993: 44: 50. © Munksgaard, 1993Keywords
This publication has 3 references indexed in Scilit:
- EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) is on 7p11.2‐q21.3Clinical Genetics, 1992
- Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe poolHuman Genetics, 1992
- EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) with a balanced reciprocal translocation between 7q11.21 and 9p12 (or 7p11.2 and 9q12) in three generationsClinical Genetics, 1991