Lammer, E J

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