- Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3S Spranger
Center for Human Genetics and Genetic Counseling, University of Bremen, Germany
Am J Med Genet 83:367-71. 1999..We discuss the phenotype in relationship to hitherto published cases with chromosomal aberrations and contiguous gene syndromes of Xp22.3...
- Interstitial deletion of 5q33.3q35.1 in a girl with mild mental retardationS Spranger
Center for Human Genetics and Genetic Counselling, University of Bremen, Germany
Am J Med Genet 93:107-9. 2000..But severe mental retardation seems to be a consistent manifestation. We describe a 4-year-old girl with a de novo deletion of 5q33.3q35.1 presenting only with mild psychomotor delay, minor facial anomalies, and seizures...