Coriell Institute for Medical Research

Biobank
Research
Services
Ordering
About Us

search submit

Clear Filter

Content Category:

apply

Samples (24227)
Website Content (1322)

Product:

apply

DNA (10713)
LCL (9581)
Fibroblast (3333)
iPSC (151)
Somatic cell hybrid (91)
Amniotic fluid-derived cell line (55)
Smooth muscle (55)
High Molecular Weight DNA (51)
Endothelial (37)
Melanocyte (35)
Keratinocyte (31)
Adipose stromal cell (22)
Preprocessed DNA (21)
mESC (12)
Epithelial (8)
Tumor-derived cell line (7)
Chorionic villus-derived cell line (4)
Hybridoma (3)
Myeloma (3)
Antibodies (2)
Mesothelial (2)
Neuronally-derived (2)
Plasmid (2)
Antigen (1)
Erythroleukemic cell line (1)
Kidney-derived cell line (1)
Microcell hybrid (1)
hybrid regional mapping panel (1)

Source:

apply

B-Lymphocyte (9622)
LCL (7032)
Whole Blood (2549)
Fibroblast (1139)
Skin, Arm (565)
Skin, Unspecified (387)
Skin, Skin (166)
Skin, Foreskin (123)
Lung, Lung (96)
Somatic cell hybrid (81)
Skin, Ear (64)
Aorta, thoracic (56)
Amniotic fluid (54)
Skin, Thigh (40)
Blood (32)
Amniotic fluid-derived cell line (23)
Skin, Abdomen (18)
Trachealis muscle (12)
Skin, Posterior iliac crest (10)
Artery, pulmonary (9)
Fetal, Unspecified (9)
Gonad, Gonad (9)
Skin, Thorax/abdomen (9)
Umbilical Cord, Umbilical cord (9)
Skin, Buttock-thigh (8)
Skin, Thorax (8)
Skin, Buttock (7)
Artery, iliac (6)
Skin, Back (6)
Skin, Sacrum (6)
Whole embryo, Embryo (6)
Conjunctiva, Conjunctiva (5)
Placental, Placenta (5)
Skin, Fetal (5)
Skin, Inguinal area (5)
Skin, Leg (5)
Vein, iliac (5)
Chorionic villus (4)
Eye (4)
Liver, Liver (4)
Muscle, Unspecified (4)
Stem cell (4)
Chorionic villus-derived cell line (3)
Epithelial (3)
Gonad, Ovary (3)
Gonad, Testes (3)
Kidney, Kidney (3)
Retina of eye (3)
Skin, Right ischium (3)
Amnion, Amnion (2)
Bladder carcinoma (2)
Brain striatum (2)
Heart, Pericardium (2)
Skin, Genital area (2)
Skin, Labialscrotal fold (2)
Spleen, Keloid (2)
T-Lymphocyte (2)
Tendon, Achilles tendon (2)
Umbilical Cord, Vein, umbilical (2)
Adenocarcinoma (1)
Adrenal cortex tumor (1)
Aorta, abdominal (1)
Aortic arch (1)
Artery, Aorta, thoracic (1)
Artery, carotid (1)
Ascites fluid (1)
Brain, Brain (1)
Brain, Unspecified (1)
Breast organoid (1)
Cartilage, Nasal (1)
Cartilage, Unspecified (1)
Cervix, Cerivix uteri (1)
Chest (1)
Cornea, Cornea (1)
Endometrial, Uterus (1)
Endothelial (1)
Fetal, Arm (1)
Gingival, Gum (1)
Heart, Unspecified (1)
Hydatidiform mole (1)
Kidney (1)
Lens, Eye (1)
Lung (1)
Mesothelial (1)
Skin, Axilla (1)
Skin, Calf (1)
Skin, Chest (1)
Skin, Embryo (1)
Skin, Foot (1)
Skin, Neck (1)
Skin, Omentum (1)
Skin, Sacral area (1)
Skin, Scalp (1)
Skin, Toe (1)
Skin, Umbilical area (1)
Tumor (1)
Tumor, Fibroma (1)
Tumor, Hepatoblastoma (1)
Tumor, Neurofibroma (1)
Tumor-derived cell line (1)

Repository:

apply

NIGMS Human Genetic Cell Repository (11106)
NINDS Repository (8393)
NHGRI Sample Repository for Human Genetic Research (2263)
NIA Aging Cell Culture Repository (2137)
Autism (262)
NIAID - USIDnet (28)
Centers for Disease Control and Prevention Repository (16)
Orphan Disease Center (13)
HD Community Biorepository (7)
Allen Cell Collection (2)

Sex:

apply

Male (12182)
Female (11735)
Other (22)

Race:

apply

White (16309)
Black/African American (1227)
More than one race (327)
Asian (298)
Other (287)
Caucasian (229)
Hispanic/Latino (189)
Unknown (171)
Asiatic Indian (110)
Chinese (78)
American Indian/Alaska Native (43)
East Indian (42)
Not Reported (39)
Asian, Other (22)
Native Hawaiian/Other Pacific Islander (15)
Filipino (7)
Korean (5)
Japanese (3)
Vietnamese (1)

Affected:

apply

Yes (13917)
No (4365)
Unknown (712)
At Risk (496)

Mutation Data Available:

apply

N (20476)
Y (3750)
No (1)

Age at Sampling (Years):

apply

0-4 (3850)
5-14 (2168)
15-24 (1769)
25-34 (2041)
35-44 (2270)
45-54 (2510)
55-64 (2506)
65-74 (1829)
75-89 (963)
90-99 (159)
100+ (60)

Collection:

apply

Heritable Diseases (8095)
Motor Neuron Disease (3940)
NHGRI Sample Repository for Human Genetic Research (2263)
Cerebrovascular Disease (2059)
Chromosome Abnormalities (1899)
Epilepsy (1298)
Apparently Healthy Collection (934)
PIGI Consented Sample (785)
dbGaP (757)
Human Variation (687)
Lysosomal Storage Diseases (684)
CEPH (662)
Muscular Dystrophies (528)
Old Order Amish Major Affective Disorder (436)
Parkinsonism (373)
Animals (338)
Repository Linkage Families (332)
GeT-RM Samples (311)
Dystonia (309)
GRC (303)
Tourette Syndrome (257)
CMD Specific (251)
Hereditary Cancers (245)
Canadian Alzheimer Disease (227)
Control (224)
Maturity-Onset Diabetes of the Young (222)
University of Georgia Centenarian Study (182)
Hybrids (172)
"Intra-abdominal fat and risk of disease in children and adolescents" study (146)
Pharmacogenetics (145)
Retinitis Pigmentosa Foundation Collection (142)
Alzheimer's Disease (137)
Venezuelan Huntington Disease (119)
Disorders of the Urea Cycle (115)
FOXG1 (93)
The 90+ Study (68)
Nonhuman Primates (61)
Italian Alzheimer Disease (58)
German Alzheimer Disease (50)
DGAP (49)
Ames Dwarf Mice (47)
Aged Sib Pairs (45)
Apparently healthy iPSCs (13)
Gene-Edited hiPSC (13)
Engineered Cell Cultures (12)
Stem Cell Collection (12)
Whole-Genome Sequence (12)
Alzheimer Disease With No Family History (11)
Specially Characterized Fibroblasts (11)
Non-Healing Wound Collection (9)
Frontotemporal Degeneration (2)
Prostate Cancer (1)

dbGap Data Available:

apply

No (22334)
Yes (1893)

Extended Clinical Data Available:

apply

No (15310)
Yes (8917)

Clear Filter

Search Results for - CONGENITAL ADRENAL HYPERPLASIA, TYPE 4

Add Quotes

(and perform an exact match search)

Please select the fields to export

All Fields
Quick View
ID
Repository
Description
Product
Source
Affected
Gene
Mutations
Sex
Age at Sampling
Race
Ethnicity
Family
Relationship To Proband
Karyotype
Publications Cited
db Gap
Supplement
Diagnosis Age
Publications
Class
Biopsy Source
Brief Description
Chromosomal Location
Collection
Cytogenetics
Rsid
Allelic Variant 1
Construct Name
Insert Length
Vector
Concentration
Sequence
Cloning Information
Gene Bank
Mutation Description
Remarks
Hispanic Ethnicity
Country of Origin
Family Member Number
Class
Alternate IDs
Biopsy Source
Cell Type
Tissue Type
Transformant
Alias
Sample Source
Species
Common Name
Subject Type
Years Longitudinal Data
Subject Currect Age
Onset Age
External Links
PDL at Senescence
Pdl at Freeze
Passage Frozen
Supplement
Cumulative PDL at Freeze
Split Ratio
Temperature
Percent CO2
Percent O2
Medium
Serum
Substrate
Sub Cult Method
Detailed Clinical Data

← Use filters to refine search | Additional fields available - click "Fields" button

Catalog Items
Documents (1322)

Loading ...

Viewing 1 - 50 of 24227 Results

Selected Items: 0

Page Size:

Reset
Repository
Description
Product
Source
Affected
Gene
Mutations
Sex
Age at Sampling
Race
Ethnicity
Family
Relationship To Proband
Karyotype

Quick View

Description

Product

Source

(Showing Items: 50)

View

NA13350

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY

DNA

LCL

View

GM13350

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY

LCL

B-Lymphocyte

View

GM13365

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY

Fibroblast

View

NA13365

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY

DNA

Fibroblast

View

GM02241

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2

Fibroblast

View

NA02241

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2

DNA

Fibroblast

View

GM02242

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2

LCL

B-Lymphocyte

View

NA02242

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2

DNA

LCL

View

NA14734

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2

DNA

LCL

View

GM14734

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2

LCL

B-Lymphocyte

View

HM12217

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2

High Molecular Weight DNA

B-Lymphocyte

View

NA12217

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2

DNA

LCL

View

NA11781

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2

DNA

LCL

View

GM11781

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2

LCL

B-Lymphocyte

View

GM12217

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2

LCL

B-Lymphocyte

View

GM14732

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY

LCL

B-Lymphocyte

View

NA14732

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY

DNA

LCL

View

NA14733

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY

DNA

LCL

View

GM23896

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY

LCL

B-Lymphocyte

View

GM14733

ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY

LCL

B-Lymphocyte

View

GM24520

ADRENAL HYPOPLASIA, CONGENITAL; AHC

LCL

B-Lymphocyte

View

GM09964

ADRENAL HYPOPLASIA, CONGENITAL; AHC

Fibroblast

View

GM23960

ADRENAL HYPOPLASIA, CONGENITAL; AHC

LCL

B-Lymphocyte

View

GM09965

ADRENAL HYPOPLASIA, CONGENITAL; AHC

Fibroblast

View

GM25222

ADRENAL HYPOPLASIA, CONGENITAL; AHC

LCL

B-Lymphocyte

View

GM23910

ADRENAL HYPOPLASIA, CONGENITAL; AHC | NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 1; NR0B1

LCL

B-Lymphocyte

View

GM25221

ADRENAL HYPOPLASIA, CONGENITAL; AHC

LCL

B-Lymphocyte

View

NA23908

ADRENAL HYPOPLASIA, CONGENITAL; AHC | NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 1; NR0B1

DNA

LCL

View

GM25223

ADRENAL HYPOPLASIA, CONGENITAL; AHC

LCL

B-Lymphocyte

View

GM23909

ADRENAL HYPOPLASIA, CONGENITAL; AHC | NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 1; NR0B1

LCL

B-Lymphocyte

View

NA23910

ADRENAL HYPOPLASIA, CONGENITAL; AHC | NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 1; NR0B1

DNA

LCL

View

GM24519

ADRENAL HYPOPLASIA, CONGENITAL; AHC

LCL

B-Lymphocyte

View

GM23908

ADRENAL HYPOPLASIA, CONGENITAL; AHC | NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 1; NR0B1

LCL

B-Lymphocyte

View

NA24519

ADRENAL HYPOPLASIA, CONGENITAL; AHC

DNA

LCL

View

GM25207

ADRENAL HYPOPLASIA, CONGENITAL; AHC

LCL

B-Lymphocyte

View

GM10490

ADRENAL HYPOPLASIA, CONGENITAL; AHC

LCL

B-Lymphocyte

View

GM08788

ADRENAL HYPOPLASIA, CONGENITAL; AHC

Fibroblast

View

NA10490

ADRENAL HYPOPLASIA, CONGENITAL; AHC

DNA

LCL

View

GM10489

ADRENAL HYPOPLASIA, CONGENITAL; AHC

LCL

B-Lymphocyte

View

NA16810

COMPLETE PATERNAL UNIPARENTAL DISOMY | COPY NUMBER VARIATION (CNV) REFERENCE PANEL 02

DNA

LCL

View

GM16810

COMPLETE PATERNAL UNIPARENTAL DISOMY | COPY NUMBER VARIATION (CNV) REFERENCE PANEL 02

LCL

B-Lymphocyte

View

GM25205

ADRENAL HYPOPLASIA, CONGENITAL; AHC

LCL

B-Lymphocyte

View

GM20615

NEPHROSIS 1, CONGENITAL, FINNISH TYPE; NPHS1

LCL

B-Lymphocyte

View

GM24521

ADRENAL HYPOPLASIA, CONGENITAL; AHC

LCL

B-Lymphocyte

View

NA24521

ADRENAL HYPOPLASIA, CONGENITAL; AHC

DNA

LCL

View

NA09285

TRANSLOCATED CHROMOSOME

DNA

Fibroblast

View

GM09285

TRANSLOCATED CHROMOSOME

Fibroblast

View

GM03852

LEBER CONGENITAL AMAUROSIS 1; LCA1

Fibroblast

View

GM20950

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id | ALG3, S. CEREVISIAE, HOMOLOG OF; ALG3

Fibroblast

Skin, Unspecified

View

GM16627

NEPHROSIS 1, CONGENITAL, FINNISH TYPE; NPHS1

Fibroblast

Skin, Thorax

No Results were Found

Show More Results

Viewing 1 - 50 of 24227 Results

Selected Items: 0

Page Size:

Repository

View Full Sample Details Add To Cart

CORIELL RESEARCH SERVICES

Apart from our online Catalog, Coriell also offers the greater scientific community a wide range of laboratory services. Our custom services include iPSC services, R&D services, assay development, custom lab services, genomic services, bioinformatic analysis, etc., to name a few.

Learn More
(Open in New Tab)

Our mission is to prevent and cure disease through biomedical research.

CUSTOMER SERVICE
customerservice@coriell.org (800) 752-3805 ● (856) 757-4848
Subscribe to our newsletter here

Coriell Institute for Medical Research
403 Haddon Avenue Camden, NJ 08103, USA (856) 966-7377

Facebook
Linkedin
Youtube