Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype.

Swinkels, Mariëlle E M

Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype. [electronic resource] - American journal of medical genetics. Part A Jun 2008 - 1430-8 p. digital

Publication Type: Journal Article

1552-4833

10.1002/ajmg.a.32310 doi


Adult
Child
Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 9--genetics
Craniofacial Abnormalities--genetics
Cytokines--genetics
DNA Mutational Analysis
Female
Humans
In Situ Hybridization, Fluorescence
Infant, Newborn
Intellectual Disability--genetics
Male
Muscle Hypotonia--genetics
Netherlands
Phenotype
Syndrome