Coriell Institute for Medical Research
Request a Quote
Careers
Login
View Cart
Samples
OR
Website
Search Help?
Sample Catalog
|
Custom Services
|
Core Facilities
|
Genomic Data Search
Navigation Header
Biobank
NIGMS
NINDS
NIA
NHGRI
Allen Cell Collection
Rett Syndrome iPSC Collection
Autism Research Resource
HD Community Biorepository
CDC Cell and DNA
NEI
J. Craig Venter Institute
Orphan Disease Center Collection
Phase Clinical Services
All Biobanks
Research
Overview
Meet Our Scientists
Our Faculty
Our Scientific Staff
Camden Cancer Research Center
Epigenetic Therapies SPORE
Core Facilities
Epigenomics
Camden Opioid Research Initiative (CORI)
The Issa & Jelinek Lab
The Jian Huang Lab
The Luke Chen Lab
The Lab
The Team
Publications
The Scheinfeldt Lab
The Shumei Song Lab
The Nora Engel Lab
The Lab
The Team
Publications
Coriell Personalized Medicine Collaborative (CPMC)
Publications
Services
Stem Cells
Core Facilties
Overview
Animal and Xenograft
Bioinformatics and Biostatistics
Cell Imaging
CRISPR Gene Engineering
Flow Cytometry and Cell Sorting
Genomics and Epigenomics
iPSC - Induced Pluripotent Stem Cells
Organoids
Biobanking and Distribution
Biobanking
Biological and Pharmaceutical Storage
Collection Kits
Coriell Marketplace
Research Support Services
Sample Procurement
Cellular and Molecular Analysis
Genomic and Epigenomic Services
Nucleic Acid Isolation and Quality Control
Customized Experimental Design and Research Solutions
Biomarkers
Cell Culture
Research and Development Models
Browse
Stem Cells
Cell Lines
DNA and RNA
Featured Products
FFPE
HMW DNA
Genomic Data Search
Diseases
Rare Diseases
Species
Gene Variants, Mutations
Notable Collections
GRC
REGARDS
Amish Major Affective Disorders
Longevity Research
Search by Catalog ID
Search Help
Ordering
Create Account
Order Online
Ordering FAQ
FAQs/Culture Instructions
Reference Materials
Biobanks
NIGMS Repository
NHGRI Repository
NINDS Repository
NIA Repository
NIST
GeT-RM
Secondary Distribution Policies
MTA Assurance Form
Shipment Policy
Contact Customer Service
Donate
Our Message
Your Impact
Giving FAQs
Make a Donation
About Us
Our History
Meet Our Team
Meet Our Board
Education
Science Fair
Summer Experience
Outreach
Research Program Internship
Press Room
Press Releases
Coriell Blog
Annual Report
Careers
Working at Coriell
Current Openings
Giving
Our Message
Your Support in Action
Giving FAQ
Giving Tuesday
Contact Us
Legal Notice
Login
View Cart
search submit
ND20098
DNA
from
Whole Blood
Description:
ASYMPTOMATIC OR UNDIAGNOSED AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL
TOURETTE SYNDROME
Affected:
At Risk
Gender:
Female
Age:
47
YR
(At Sampling)
Sample Description
Overview
Phenotypic Data
External Links
Overview
Repository
NINDS Repository
Subcollection
Tourette Syndrome
Quantity
3 µg
Quantitation Method
Please see our
FAQ
Biopsy Source
Peripheral vein
Sample Source
DNA from Whole Blood
Race
White
Subject Type
parent/child discordant pair
Family Type
NUCLEAR FAMILIES - ONE AFFECTED
Ethnicity
Not Hispanic/Latino
Country of Origin
USA
Family Member
2
Family History
N
Relation to Proband
mother
Species
Homo
sapiens
Common Name
Human
Note
This material represents a finite resource (DNA from Whole Blood)
Phenotypic Data
Demographic Data
Relation to Proband
mother
Age at Sampling
47 YR
Gender
Female
Age of Onset(If not a control)
No Data
Age at Diagnosis(If not a control)
No Data
Hispanic or Latino/Not Hispanic or Latino
Not Hispanic/Latino
Racial Category
White
Country
USA
Diagnosed By
No Data
Data Elements
Clinical Element Type: Tourettes
(Baseline)
Primary Lifetime Clinical Diagnosis
Tourette’s Disorder
present
absent
Chronic Multiple Tics
present
absent
Other Tic disorder
present
absent
Unaffected or undiagnosed primary blood relative of proband
yes
no
Symptoms: Motor Tics
present
absent
Symptoms: Vocal/Verbal Tics
present
absent
Age at Tic onset
No Data
Genetic Data of Subject
Mutation/s in subject's DNA (if present, describe)
present
absent
unknown
Secondary Lifetime Clinical Diagnosis
Obsessive compulsive disorder
present
absent
Attention Deficit/Hyperactivity Disorder
present
absent
Other (specify)
present
absent
Optional data
Handedness
Right
Left
Ambidextrous
smoking history
never
former smoker
current smoker
years smoking
2
Other family members
Other family members of this person in NINDS repository
yes
no
Notes:
SON ND20097
Family History of TS and related disorders in first degree relatives of subject
Tourette Syndrome or tic disorders
present
absent
Notes:
SON ND20097
Obsessive Compulsive Disorder (OCD)
present
absent
Attention Deficit Hyperactivity Disorder (ADHD)
present
absent
List all first degree relatives and diagnosis (TS, tic disorder, OCD, ADHD)
SON TOURETTE (ND20097)
Family History of Neurological Disease in first degree relatives
Motor Neuron Disorders, including ALS
present
absent
Parkinson’s disease
present
absent
Epilepsy
present
absent
Cerebrovascular Disorders, including stroke and aneurysm
present
absent
External Links
NCBI Gene
Gene ID:2973
NCBI GTR
137580 GILLES DE LA TOURETTE SYNDROME; GTS
OMIM
137580 GILLES DE LA TOURETTE SYNDROME; GTS
Culture Protocols
Supplement
-
Pricing
Commercial and Non-U.S.:
$0.00
USD
U.S. Academic or
Non-profit:
$0.00
USD
NINDS Repository Submitter (past or current) and/or Current NINDS Grantee
$0.00
USD
Add to Cart
How to Order
Ordering Instructions
MTA / Assurance Form
Statement of Research Intent Form
Related Products
Same Family
NINDS1776