TY  - GEN
AU  - Swinkels,Mariëlle E M
AU  - Simons,Annet
AU  - Smeets,Dominique F
AU  - Vissers,Lisenka E
AU  - Veltman,Joris A
AU  - Pfundt,Rolph
AU  - de Vries,Bert B A
AU  - Faas,Brigitte H W
AU  - Schrander-Stumpel,Connie T R M
AU  - McCann,Emma
AU  - Sweeney,Elizabeth
AU  - May,Paul
AU  - Draaisma,Jos M
AU  - Knoers,Nine V
AU  - van Kessel,Ad Geurts
AU  - van Ravenswaaij-Arts,Conny M A
TI  - Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype
SN  - 1552-4833
PY  - 2008///0626
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 9
KW  - genetics
KW  - Craniofacial Abnormalities
KW  - Cytokines
KW  - DNA Mutational Analysis
KW  - Female
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Infant, Newborn
KW  - Intellectual Disability
KW  - Male
KW  - Muscle Hypotonia
KW  - Netherlands
KW  - Phenotype
KW  - Syndrome
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1002/ajmg.a.32310
ER  -