Clear Filter
  • (1379)
  • (520)
  • (563)
  • (401)
  • (362)
  • (41)
  • (9)
  • (1)
  • (1)
  • (1)
  • (570)
  • (228)
  • (164)
  • (84)
  • (46)
  • (40)
  • (10)
  • (3)
  • (2)
  • (2)
  • (2)
  • (2)
  • (2)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1329)
  • (43)
  • (3)
  • (2)
  • (2)
  • (734)
  • (639)
  • (4)
  • (982)
  • (71)
  • (24)
  • (22)
  • (20)
  • (15)
  • (11)
  • (10)
  • (9)
  • (8)
  • (5)
  • (4)
  • (4)
  • (2)
  • (2)
  • (1)
  • (1)
  • (884)
  • (212)
  • (7)
  • (6)
  • (815)
  • (564)
  • (424)
  • (280)
  • (167)
  • (121)
  • (133)
  • (100)
  • (33)
  • (22)
  • (4)
  • (1)
  • (2)
  • (1044)
  • (386)
  • (275)
  • (183)
  • (179)
  • (120)
  • (93)
  • (19)
  • (16)
  • (14)
  • (13)
  • (9)
  • (6)
  • (3)
  • (3)
  • (3)
  • (3)
  • (2)
  • (2)
  • (2)
  • (2)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1379)
  • (1276)
  • (103)
  Clear Filter

Search Results for - CONGENITAL SMALL ADRENAL GLAND

 Use filters to refine search | Additional fields available - click "Fields" button
Loading ...
1 - 50 of 1379 Results
Selected Items: 0
Page Size:
 
 
Quick View
 
ID
 
Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
Fibroblast
 
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
Fibroblast
 
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
DNA
 
LCL
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
Fibroblast
 
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC | NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 1; NR0B1
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC | NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 1; NR0B1
 
DNA
 
LCL
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC | NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 1; NR0B1
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC | NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 1; NR0B1
 
DNA
 
LCL
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC | NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 1; NR0B1
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
DNA
 
LCL
 
 
 
 
ADRENAL HYPOPLASIA, CONGENITAL; AHC
 
DNA
 
LCL
 
 
 
 
HYPERGLYCEROLEMIA | GLYCEROL KINASE; GK
 
DNA
 
LCL
 
 
 
 
HYPERGLYCEROLEMIA | GLYCEROL KINASE; GK
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2
 
DNA
 
LCL
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY
 
DNA
 
LCL
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY
 
DNA
 
LCL
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY
 
LCL
 
B-Lymphocyte
 
 
 
 
ANEUPLOID CHROMOSOME NUMBER - TRISOMY 9 | ANEUPLOID CHROMOSOME NUMBER - TRISOMY
 
Fibroblast
 
 
 
 
 
ANEUPLOID CHROMOSOME NUMBER - TRISOMY 9 | ANEUPLOID CHROMOSOME NUMBER - TRISOMY
 
DNA
 
Fibroblast
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2
 
High Molecular Weight DNA
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2
 
DNA
 
LCL
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2
 
DNA
 
LCL
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2
 
Fibroblast
 
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2
 
DNA
 
Fibroblast
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2
 
DNA
 
LCL
 
 
 
 
CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1
 
Fibroblast
 
Skin, Arm
 
 
 
 
CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1
 
LCL
 
B-Lymphocyte
 
 
 
 
ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAA | AAAS GENE; AAAS
 
Fibroblast
 
Muscle, Unspecified
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY
 
DNA
 
LCL
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY
 
Fibroblast
 
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY
 
LCL
 
B-Lymphocyte
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY
 
DNA
 
Fibroblast
 
 
 
 
CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1
 
DNA
 
LCL
 
 
 
 
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY | CYTOCHROME P450, FAMILY 21, SUBFAMILY A, POLYPEPTIDE 2; CYP21A2
 
LCL
 
B-Lymphocyte

No Results were Found

1 - 50 of 1379 Results
Selected Items: 0
Page Size:

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)
Footer

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

CONTACT US

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

Ⓒ 2025 Coriell Institute. All rights reserved.