Abstract
The deletion of 4q31→qter is associated with a recognizable '4q- syndrome'. It has been proposed that the much rarer deletion 4q33→qter causes a milder phenotypic expression of the 4q- syndrome. We present the second case, the first male, with the latter deletion and compare his clinical features to those of other 4q- patients.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 125-129 |
| Number of pages | 5 |
| Journal | Clinical Genetics |
| Volume | 21 |
| Issue number | 2 |
| State | Published - 1982 |
ASJC Scopus subject areas
- Genetics
- Genetics(clinical)