Terminal deletion(4)(q33) in a male infant
- 1 February 1982
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 21 (2) , 125-129
- https://doi.org/10.1111/j.1399-0004.1982.tb00748.x
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.Keywords
This publication has 4 references indexed in Scilit:
- Deletions of different segments of the long arm of chromosome 4American Journal of Medical Genetics, 1981
- The del(4) (q31) syndrome‐A recognizable disorder with atypical Robin malformation SequenceAmerican Journal of Medical Genetics, 1981
- A new R-banding technique in clinical cytogeneticsHuman Genetics, 1980
- 4q- SyndromeArchives of Pediatrics & Adolescent Medicine, 1979