Clinical findings and phenotype in a toddler with 48,XXYY syndrome
- 10 April 2003
- journal article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 119A (3) , 393-394
- https://doi.org/10.1002/ajmg.a.20015
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Rare sex chromosome aneuploidies in humans: Report of six patients with 48,XXYY, 49,XXXXY, and 48,XXXX karyotypesAmerican Journal of Medical Genetics, 1999
- Verbal deficits in children with 47, XXY and 47, XXX karyotypes: A descriptive and experimental studyBrain and Language, 1982
- Sex chromosome aberrations and speech development.Archives of Disease in Childhood, 1973
- Do the 48, XXYY males have a characteristic phenotype? A ReviewClinical Genetics, 1970
- The 48, XXYY syndromeThe American Journal of Medicine, 1970