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Search Results for -
XP, GROUP A
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XERODERMA PIGMENTOSUM I
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A
XP1
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Repository:
NIGMS Human Genetic Cell Repository
(6414)
NINDS Repository
(4685)
NIA Aging Cell Culture Repository
(2240)
HD Community Biorepository
(140)
NHGRI Sample Repository for Human Genetic Research
(64)
NIAID - USIDnet
(27)
Centers for Disease Control and Prevention Repository
(24)
Autism
(2)
Orphan Disease Center
(2)
Allen Cell Collection
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Collection:
Heritable Diseases
(5210)
Cerebrovascular Disease
(1974)
Parkinsonism
(1080)
Apparently Healthy Collection
(801)
GRC
(756)
Chromosome Abnormalities
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PIGI Consented Sample
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Tourette Syndrome
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Canadian Alzheimer Disease
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dbGaP
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Venezuelan Huntington Disease
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Alzheimer's Disease
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Pharmacogenetics
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University of Georgia Centenarian Study
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CMD Specific
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CEPH
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"Intra-abdominal fat and risk of disease in children and adolescents" study
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Disorders of the Urea Cycle
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Retinitis Pigmentosa Foundation Collection
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Old Order Amish Major Affective Disorder
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Whole-Genome Sequence
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Ames Dwarf Mice
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FOXG1
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Maturity-Onset Diabetes of the Young
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Alzheimer Disease With No Family History
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Apparently healthy iPSCs
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Nonhuman Primates
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Engineered Cell Cultures
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Specially Characterized Fibroblasts
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Non-Healing Wound Collection
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DGAP
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FFPE
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Microcell hybrid
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Myeloma
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Affected:
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No
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At Risk
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Unknown
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Mutation Data Available:
N
(9658)
Y
(3941)
Source:
B-Lymphocyte
(4990)
LCL
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Whole Blood
(1711)
Skin, Arm
(944)
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Skin, Unspecified
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Skin, Skin
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Brain striatum
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Skin, Sacrum
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Breast organoid
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Embryonal carcinoma
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Eye
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Male
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More than one race
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Chinese
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Korean
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dbGap Data Available:
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(13176)
Yes
(423)
Extended Clinical Data Available:
No
(8599)
Yes
(5000)
Age at Sampling (Years):
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35-44
(1710)
55-64
(1598)
5-14
(1518)
25-34
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15-24
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0-4
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