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Search Results for -
XP, GROUP A
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Also searched for:
XERODERMA PIGMENTOSUM I
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A
XP1
XPA
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Repository:
NIGMS Human Genetic Cell Repository
(6672)
NINDS Repository
(4694)
NIA Aging Cell Culture Repository
(2347)
HD Community Biorepository
(140)
NHGRI Sample Repository for Human Genetic Research
(65)
Centers for Disease Control and Prevention Repository
(24)
Orphan Disease Center
(6)
Allen Cell Collection
(3)
Autism
(2)
Collection:
Heritable Diseases
(5491)
Cerebrovascular Disease
(1975)
Parkinsonism
(1083)
Apparently Healthy Collection
(804)
GRC
(782)
Chromosome Abnormalities
(671)
PIGI Consented Sample
(666)
Epilepsy
(571)
Lysosomal Storage Diseases
(549)
Human Variation
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Motor Neuron Disease
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Tourette Syndrome
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GeT-RM Samples
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Control
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Animals
(209)
Canadian Alzheimer Disease
(208)
Venezuelan Huntington Disease
(193)
Dystonia
(191)
Alzheimer's Disease
(182)
dbGaP
(172)
CMD Specific
(162)
University of Georgia Centenarian Study
(142)
Retinitis Pigmentosa Foundation Collection
(137)
Pharmacogenetics
(129)
CEPH
(106)
"Intra-abdominal fat and risk of disease in children and adolescents" study
(98)
Disorders of the Urea Cycle
(95)
German Alzheimer Disease
(87)
Italian Alzheimer Disease
(68)
NHGRI Sample Repository for Human Genetic Research
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Old Order Amish Major Affective Disorder
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Whole-Genome Sequence
(53)
Repository Linkage Families
(48)
Aged Sib Pairs
(47)
Ames Dwarf Mice
(47)
FOXG1
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Maturity-Onset Diabetes of the Young
(31)
Alzheimer Disease With No Family History
(29)
Apparently healthy iPSCs
(26)
Nonhuman Primates
(16)
Engineered Cell Cultures
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Gene-Edited hiPSC
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Specially Characterized Fibroblasts
(11)
Non-Healing Wound Collection
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DGAP
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Frontotemporal Degeneration
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Product:
DNA
(5741)
LCL
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iPSC
(170)
Plasmid
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Endothelial
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High Molecular Weight DNA
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Smooth muscle
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Adipose stromal cell
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Epithelial
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Protein
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Mesothelial
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(1)
Erythroleukemic cell line
(1)
FFPE
(1)
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(1)
Melanocyte
(1)
Microcell hybrid
(1)
Myeloma
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Affected:
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(7153)
No
(3155)
At Risk
(1711)
Unknown
(172)
Mutation Data Available:
N
(9683)
Y
(4270)
Source:
B-Lymphocyte
(5022)
LCL
(3167)
Whole Blood
(1714)
Skin, Arm
(945)
Fibroblast
(832)
Skin, Unspecified
(298)
Somatic cell hybrid
(142)
Skin, Skin
(137)
Lung, Lung
(62)
Skin, Ear
(58)
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(33)
Aorta, thoracic
(27)
Blood
(24)
Amniotic fluid
(13)
Brain striatum
(13)
Skin, Abdomen
(13)
Trachealis muscle
(12)
Vein, iliac
(11)
Amniotic fluid-derived cell line
(9)
Artery, iliac
(8)
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Skin, Buttock
(7)
Skin, Sacrum
(7)
Breast organoid
(6)
Stem cell
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Epithelial
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Skin, Foreskin
(5)
Umbilical Cord, Umbilical cord
(5)
Embryonal carcinoma
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Eye
(4)
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(4)
Skin, Back
(4)
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(4)
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(4)
Fetal, Unspecified
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Gonad, Ovary
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Skin, Right ischium
(3)
Artery, pulmonary
(2)
Bladder carcinoma
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Chorionic villus
(2)
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Endometrial, Uterus
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Gonad, Gonad
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Kidney
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Liver, Liver
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Lung
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Muscle, Unspecified
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Skin, Fetal
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Skin, Hip
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Skin, Thorax
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Tumor-derived cell line
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Whole embryo, Embryo
(2)
Adenocarcinoma
(1)
Adrenal cortex tumor
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Aorta, abdominal
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Ascites fluid, Ascites fluid
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Brain, Unspecified
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Cartilage, Nasal
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Cartilage, Unspecified
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Cervix, Cerivix uteri
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Endothelial
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Fetal, Arm
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Gingival, Gum
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Heart, Pericardium
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Peripheral Vein
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Skin, Breast
(1)
Skin, Calf
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Skin, Scalp
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Skin, Thoraco-lumbar junction
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Skin, Toe
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Smooth muscle
(1)
Spleen, Keloid
(1)
Tendon, Achilles tendon
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Tendon, Leg
(1)
Tumor
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Tumor, Abdomen
(1)
Tumor, Adenoma
(1)
Tumor, Fibroma
(1)
Tumor, Hepatoblastoma
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Vein, umbilical
(1)
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(6992)
Male
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Other
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(10261)
Black/African American
(655)
Asian
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Asiatic Indian
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More than one race
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Unknown
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Not Reported
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(16)
Asian, Other
(15)
Chinese
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Filipino
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Caucasian
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Japanese
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Korean
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dbGap Data Available:
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(13510)
Yes
(443)
Extended Clinical Data Available:
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(8888)
Yes
(5065)
Age at Sampling (Years):
45-54
(1885)
35-44
(1779)
55-64
(1631)
5-14
(1562)
25-34
(1392)
15-24
(1355)
0-4
(1216)
65-74
(985)
75-89
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100+
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