Inherited duplication of Xq27.2-->qter: phenocopy of infantile Prader-Willi syndrome. [electronic resource]
- Clinical dysmorphology Apr 2001
- 141-4 p. digital
Publication Type: Case Reports; Journal Article
0962-8827
10.1097/00019605-200104000-00012 doi
Genes, Duplicate Humans In Situ Hybridization, Fluorescence Infant Male Phenotype Prader-Willi Syndrome--genetics Sex Chromosome Aberrations--genetics X Chromosome