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

  Clear Filter
  • (1821)
  • (63)
  • (824)
  • (534)
  • (379)
  • (49)
  • (20)
  • (12)
  • (2)
  • (1)
  • (835)
  • (377)
  • (177)
  • (83)
  • (51)
  • (35)
  • (15)
  • (12)
  • (3)
  • (2)
  • (2)
  • (2)
  • (2)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1)
  • (1579)
  • (220)
  • (20)
  • (2)
  • (1031)
  • (781)
  • (4)
  • (1318)
  • (81)
  • (34)
  • (24)
  • (22)
  • (21)
  • (12)
  • (10)
  • (9)
  • (8)
  • (5)
  • (3)
  • (3)
  • (2)
  • (2)
  • (1)
  • (1)
  • (1)
  • (1233)
  • (361)
  • (11)
  • (10)
  • (1124)
  • (697)
  • (358)
  • (293)
  • (184)
  • (178)
  • (206)
  • (146)
  • (145)
  • (89)
  • (50)
  • (1377)
  • (595)
  • (341)
  • (285)
  • (258)
  • (217)
  • (100)
  • (93)
  • (86)
  • (10)
  • (6)
  • (5)
  • (4)
  • (4)
  • (3)
  • (2)
  • (2)
  • (2)
  • (1)
  • (1)
  • (1)
  • (1819)
  • (2)
  • (1528)
  • (293)
  Clear Filter

Search Results for - WALKER-WARBURG CONGENITAL MUSCULAR DYSTROPHY

Add Quotes
← Use filters to refine search | Additional fields available - click "Fields" button
Loading ...
1 - 50 of 1821 Results
Selected Items: 0
Page Size:
 
 
Quick View
 
ID
 
Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 (WALKER-WARBURG SYNDROME INCLUDED)
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4 (WALKER-WARBURG SYNDROME INCLUDED) | FUKUTIN; FKTN
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6; MDDGA6 (WALKER-WARBURG SYNDROME INCLUDED) | CHROMOSOME DELETION | ACETYLGLUCOSAMINYLTRANSFERASE-LIKE PROTEIN; LARGE1
 
DNA
 
Fibroblast
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4 (WALKER-WARBURG SYNDROME INCLUDED) | FUKUTIN; FKTN
 
Fibroblast
 
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4 (WALKER-WARBURG SYNDROME INCLUDED) | FUKUTIN; FKTN
 
DNA
 
Fibroblast
 
 
 
 
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6; MDDGA6 (WALKER-WARBURG SYNDROME INCLUDED) | CHROMOSOME DELETION | ACETYLGLUCOSAMINYLTRANSFERASE-LIKE PROTEIN; LARGE1
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A | LAMININ, ALPHA-2; LAMA2
 
Fibroblast
 
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
DNA
 
Fibroblast
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A | LAMININ, ALPHA-2; LAMA2
 
Fibroblast
 
Skin, Skin
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
DNA
 
LCL
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Skin
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
 
LCL
 
B-Lymphocyte
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1 | SELENOPROTEIN N, 1; SEPN1
 
LCL
 
B-Lymphocyte
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1
 
LCL
 
B-Lymphocyte
 
 
 
 
SELENON-RELATED MYOPATHY; RIGID SPINE MUSCULAR DYSTROPHY 1; RSMD1 | SELENOPROTEIN N, 1; SEPN1
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE VI, ALPHA-2; COL6A2
 
LCL
 
B-Lymphocyte
 
 
 
 
ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD1 | COLLAGEN, TYPE VI, ALPHA-2; COL6A2
 
LCL
 
B-Lymphocyte

No Results were Found

Show More Results
1 - 50 of 1821 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.