No abstract available
MeSH terms
-
Abnormalities, Multiple / genetics*
-
Child
-
Chromosomes, Human, Pair 14 / genetics*
-
Female
-
Genetic Markers / genetics
-
Humans
-
Infant
-
Intellectual Disability / genetics
-
Karyotyping
-
Male
-
Phenotype
-
Prader-Willi Syndrome / diagnosis
-
Prader-Willi Syndrome / genetics*
-
Translocation, Genetic