Sample Catalog | Custom Services | Core Facilities | Genomic Data Search

  Clear Filter
  • (2444)
  • (106)
  • (1119)
  • (977)
  • (323)
  • (23)
  • (1)
  • (1)
  • (1119)
  • (882)
  • (59)
  • (50)
  • (47)
  • (46)
  • (29)
  • (12)
  • (8)
  • (2)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1797)
  • (362)
  • (237)
  • (48)
  • (1232)
  • (1209)
  • (1865)
  • (312)
  • (67)
  • (25)
  • (20)
  • (14)
  • (13)
  • (8)
  • (7)
  • (6)
  • (5)
  • (5)
  • (5)
  • (1)
  • (1250)
  • (883)
  • (24)
  • (14)
  • (1918)
  • (526)
  • (200)
  • (229)
  • (351)
  • (364)
  • (367)
  • (311)
  • (258)
  • (175)
  • (106)
  • (2)
  • (1610)
  • (1009)
  • (195)
  • (148)
  • (146)
  • (76)
  • (51)
  • (34)
  • (33)
  • (24)
  • (21)
  • (21)
  • (16)
  • (15)
  • (13)
  • (11)
  • (9)
  • (7)
  • (5)
  • (5)
  • (2)
  • (2)
  • (2)
  • (2)
  • (2)
  • (1)
  • (1)
  • (1)
  • (2347)
  • (97)
  • (2076)
  • (368)
  Clear Filter

Search Results for - PEROXISOME BIOGENESIS DISORDER 3B

Add Quotes
← Use filters to refine search | Additional fields available - click "Fields" button
Loading ...
1 - 50 of 2444 Results
Selected Items: 0
Page Size:
 
 
Quick View
 
ID
 
Description
 
Product
 
Source
 
Gene
(Showing Items: 50)
 
 
 
 
REFSUM DISEASE, INFANTILE FORM
 
LCL
 
B-Lymphocyte
 
 
 
 
 
REFSUM DISEASE, INFANTILE FORM
 
Fibroblast
 
 
 
 
 
 
REFSUM DISEASE, INFANTILE FORM
 
Fibroblast
 
 
 
 
 
 
REFSUM DISEASE, INFANTILE FORM
 
LCL
 
B-Lymphocyte
 
 
 
 
 
REFSUM DISEASE, INFANTILE FORM
 
Fibroblast
 
 
 
 
 
 
REFSUM DISEASE, INFANTILE FORM | PEROXISOME BIOGENESIS FACTOR 26; PEX26
 
DNA
 
Fibroblast
 
PEX26
 
 
 
 
REFSUM DISEASE, INFANTILE FORM | PEROXISOME BIOGENESIS FACTOR 26; PEX26
 
Fibroblast
 
Skin, Arm
 
PEX26
 
 
 
 
REFSUM DISEASE, INFANTILE FORM | PEROXISOME BIOGENESIS FACTOR 26; PEX26
 
Fibroblast
 
 
PEX26
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A | PEROXISOME BIOGENESIS FACTOR 16; PEX16
 
Fibroblast
 
 
PEX16
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER); PBD4A | PEROXISOME BIOGENESIS FACTOR 6; PEX6
 
Fibroblast
 
 
PEX6
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER); PBD4A
 
Fibroblast
 
 
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER); PBD4A
 
Fibroblast
 
 
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A
 
Fibroblast
 
 
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER); PBD4A
 
Fibroblast
 
 
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A | PEROXISOME BIOGENESIS FACTOR 16; PEX16
 
DNA
 
Fibroblast
 
PEX16
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER); PBD4A | PEROXISOME BIOGENESIS FACTOR 6; PEX6
 
DNA
 
Fibroblast
 
PEX6
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A | PEROXISOME BIOGENESIS FACTOR 26; PEX26
 
DNA
 
Fibroblast
 
PEX26
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A | PEROXISOME BIOGENESIS FACTOR 26; PEX26
 
Fibroblast
 
Skin, Arm
 
PEX26
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A | PEROXISOME BIOGENESIS FACTOR 26; PEX26
 
Fibroblast
 
 
PEX26
 
 
 
 
ZELLWEGER SYNDROME; ZS | PEROXISOME BIOGENESIS FACTOR 1; PEX1
 
DNA
 
Fibroblast
 
PEX1
 
 
 
 
ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM | PEROXISOME BIOGENESIS FACTOR 26; PEX26
 
Fibroblast
 
 
PEX26
 
 
 
 
ZELLWEGER SYNDROME; ZS | PEROXISOME BIOGENESIS FACTOR 1; PEX1
 
Fibroblast
 
Skin, Unspecified
 
PEX1
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 7B; PBD7B | RETINITIS PIGMENTOSA 1; RP1 | PEROXISOME BIOGENESIS FACTOR 26; PEX26
 
Fibroblast
 
Skin, Arm
 
PEX26
 
 
 
 
ZELLWEGER SYNDROME; ZS
 
DNA
 
Fibroblast
 
 
 
 
 
ZELLWEGER SYNDROME; ZS
 
LCL
 
B-Lymphocyte
 
 
 
 
 
ZELLWEGER SYNDROME; ZS
 
DNA
 
LCL
 
 
 
 
 
ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
 
Fibroblast
 
 
 
 
 
 
ZELLWEGER SYNDROME; ZS
 
LCL
 
B-Lymphocyte
 
 
 
 
 
ZELLWEGER SYNDROME; ZS
 
Fibroblast
 
 
 
 
 
 
ZELLWEGER SYNDROME; ZS
 
Fibroblast
 
 
 
 
 
 
PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A
 
Fibroblast
 
Skin, Arm
 
 
 
 
 
ZELLWEGER SYNDROME; ZS
 
LCL
 
B-Lymphocyte
 
 
 
 
 
ZELLWEGER SYNDROME; ZS
 
Fibroblast
 
 
 
 
 
 
ZELLWEGER SYNDROME; ZS
 
DNA
 
Fibroblast
 
 
 
 
 
ZELLWEGER SYNDROME; ZS
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
 
ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
 
Fibroblast
 
Skin, Arm
 
 
 
 
 
ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
 
ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
 
Fibroblast
 
 
 
 
 
 
ZELLWEGER SYNDROME; ZS
 
Fibroblast
 
 
 
 
 
 
ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
 
ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
 
Fibroblast
 
Skin, Arm
 
 
 
 
 
ZELLWEGER SYNDROME; ZS | INVERTED CHROMOSOME
 
Fibroblast
 
 
 
 
 
 
ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM
 
Fibroblast
 
Skin, Arm
 
 
 
 
 
ADRENOLEUKODYSTROPHY; ALD | ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 1; ABCD1
 
DNA
 
Fibroblast
 
ABCD1
 
 
 
 
ADRENOLEUKODYSTROPHY; ALD | ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 1; ABCD1
 
Fibroblast
 
Skin, Arm
 
ABCD1
 
 
 
 
EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3B, SEVERE; JEB3B
 
Fibroblast
 
 
 
 
 
 
EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3B, SEVERE; JEB3B
 
LCL
 
B-Lymphocyte
 
 
 
 
 
EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3B, SEVERE; JEB3B
 
LCL
 
B-Lymphocyte
 
 
 
 
 
EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3B, SEVERE; JEB3B | APPARENTLY HEALTHY INDIVIDUAL | LAMININ, GAMMA-2; LAMC2
 
Fibroblast
 
 
LAMC2
 
 
 
 
EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3B, SEVERE; JEB3B | LAMININ, GAMMA-2; LAMC2
 
Fibroblast
 
 
LAMC2

No Results were Found

Show More Results
1 - 50 of 2444 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)
Close
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.