Home
About
Overview
Sharing Data
ORCID
Help
History (1)
IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features.
See All Pages
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features.
IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features. Eur J Med Genet. 2012 Jan; 55(1):32-6.
View in:
PubMed
subject areas
Abnormalities, Multiple
Abnormalities, Multiple
Adolescent
Adolescent
Chromosomes, Human, X
Chromosomes, Human, X
Female
Female
Gene Deletion
Gene Deletion
Genetic Testing
Genetic Testing
Hippocampus
Hippocampus
Humans
Humans
Interleukin-1 Receptor Accessory Protein
Interleukin-1 Receptor Accessory Protein
Male
Male
Mental Retardation, X-Linked
Mental Retardation, X-Linked
Oligonucleotide Array Sequence Analysis
Oligonucleotide Array Sequence Analysis
Pedigree
Pedigree
Phenotype
Phenotype