Skip to main navigation
Skip to search
Skip to main content
UTMB Health Research Expert Profiles Home
Help & FAQ
Home
Experts
Departments
Equipment
Projects/Grants
Publications
Activities
Press/Media
Honors
Impacts
Search by expertise, name or affiliation
Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders
Patrícia Bs Celestino-Soper
, Cindy Skinner
, Richard Schroer
, Patricia Eng
, Jayant Shenai
, Malgorzata M.J. Nowaczyk
, Deborah Terespolsky
, Donna Cushing
, Gayle S. Patel
, Ladonna Immken
, Alecia Willis
, Joanna Wiszniewska
, Reuben Matalon
, Jill A. Rosenfeld
, Roger E. Stevenson
, Sung Hae L. Kang
, Sau Wai Cheung
, Arthur L. Beaudet
, Pawel Stankiewicz
Research output
:
Contribution to journal
›
Article
›
peer-review
45
Scopus citations
Overview
Fingerprint
Fingerprint
Dive into the research topics of 'Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders'. Together they form a unique fingerprint.
Sort by
Weight
Alphabetically
Keyphrases
Autism Spectrum Disorder
100%
ATXN1
100%
Delay Spectrum
100%
Developmental Delay
100%
Autism
50%
South Carolina
50%
Dysmorphic Features
50%
Seizure
25%
Older Patients
25%
Short-arm
25%
Intellectual Disability
25%
Chromosome 6
25%
Hypotonia
25%
Interstitial Deletion
25%
Array Comparative Genomic Hybridization (aCGH)
25%
NHLRC1
25%
Heart Defects
25%
Database Query
25%
Submicroscopic Deletion
25%
Congenital Anomalies
25%
Language Delay
25%
Behavioral Abnormalities
25%
Defect Characteristics
25%
JARID2
25%
DTNBP1
25%
Biochemistry, Genetics and Molecular Biology
Intellectual Disability
100%
Chromosome 6
100%
Array Comparative Genomic Hybridization
100%
JARID2
100%