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On page 118 showing 2341 ~ 2360 out of 20,547 results
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  • RRID:CVCL_GS81

https://web.expasy.org/cellosaurus/CVCL_GS81

Organism: Homo sapiens (Human)
Disease: Juvenile myoclonic epilepsy
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_GS81 Copy   


  • RRID:CVCL_9Z47

https://web.expasy.org/cellosaurus/CVCL_9Z47

Organism: Homo sapiens (Human)
Disease: Refsum disease
Category: Finite cell line

Proper citation: Coriell Cat# GM13202, RRID:CVCL_9Z47 Copy   


  • RRID:CVCL_N205

https://web.expasy.org/cellosaurus/CVCL_N205

Organism: Homo sapiens (Human)
Disease: Hunter syndrome
Category: Finite cell line
Comments: Population: Caribbean; Haitian., Part of: Human variation panel.

Proper citation: RRID:CVCL_N205 Copy   


  • RRID:CVCL_H548

https://web.expasy.org/cellosaurus/CVCL_H548

Organism: Homo sapiens (Human)
Category: Finite cell line

Proper citation: RRID:CVCL_H548 Copy   


  • RRID:CVCL_X451

https://web.expasy.org/cellosaurus/CVCL_X451

Organism: Homo sapiens (Human)
Disease: Aspartylglycosaminuria
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM13201, RRID:CVCL_X451 Copy   


  • RRID:CVCL_U401

https://web.expasy.org/cellosaurus/CVCL_U401

Organism: Homo sapiens (Human)
Disease: Tay-Sachs disease
Category: Finite cell line

Proper citation: RRID:CVCL_U401 Copy   


  • RRID:CVCL_9Y33

https://web.expasy.org/cellosaurus/CVCL_9Y33

Organism: Homo sapiens (Human)
Disease: Sly syndrome
Category: Finite cell line
Comments: Population: Mexican.

Proper citation: RRID:CVCL_9Y33 Copy   


  • RRID:CVCL_4Z71

https://web.expasy.org/cellosaurus/CVCL_4Z71

Organism: Homo sapiens (Human)
Disease: Trichothiodystrophy
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM13287, RRID:CVCL_4Z71 Copy   


  • RRID:CVCL_2U25

https://web.expasy.org/cellosaurus/CVCL_2U25

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_2U25 Copy   


  • RRID:CVCL_9R32

https://web.expasy.org/cellosaurus/CVCL_9R32

Organism: Homo sapiens (Human)
Disease: Neonatal adrenoleukodystrophy
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_9R32 Copy   


  • RRID:CVCL_4F71

https://web.expasy.org/cellosaurus/CVCL_4F71

Organism: Homo sapiens (Human)
Disease: Medium-chain acyl-CoA dehydrogenase deficiency
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_4F71 Copy   


  • RRID:CVCL_IJ39

https://web.expasy.org/cellosaurus/CVCL_IJ39

Organism: Homo sapiens (Human)
Disease: Galactosialidosis
Category: Finite cell line

Proper citation: Coriell Cat# GM13206, RRID:CVCL_IJ39 Copy   


  • RRID:CVCL_4F69

https://web.expasy.org/cellosaurus/CVCL_4F69

Organism: Homo sapiens (Human)
Disease: Zellweger syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM13272, RRID:CVCL_4F69 Copy   


  • RRID:CVCL_2U24

https://web.expasy.org/cellosaurus/CVCL_2U24

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(1;13)(1pter->1q25::13q22->13qter;13pter->13q22::1q25->1qter) (Coriell=GM13238).

Proper citation: Coriell Cat# GM13238, RRID:CVCL_2U24 Copy   


  • RRID:CVCL_IJ39

https://web.expasy.org/cellosaurus/CVCL_IJ39

Organism: Homo sapiens (Human)
Disease: Galactosialidosis
Category: Finite cell line

Proper citation: RRID:CVCL_IJ39 Copy   


  • RRID:CVCL_4F66

https://web.expasy.org/cellosaurus/CVCL_4F66

Organism: Homo sapiens (Human)
Disease: Zellweger syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM13266, RRID:CVCL_4F66 Copy   


  • RRID:CVCL_4Z71

https://web.expasy.org/cellosaurus/CVCL_4Z71

Organism: Homo sapiens (Human)
Disease: Trichothiodystrophy
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: RRID:CVCL_4Z71 Copy   


  • RRID:CVCL_BW65

https://web.expasy.org/cellosaurus/CVCL_BW65

Organism: Homo sapiens (Human)
Disease: D-bifunctional protein deficiency
Category: Finite cell line
Comments: Population: African American.

Proper citation: RRID:CVCL_BW65 Copy   


  • RRID:CVCL_4F67

    This resource has 1+ mentions.

https://web.expasy.org/cellosaurus/CVCL_4F67

Organism: Homo sapiens (Human)
Disease: Zellweger syndrome
Category: Finite cell line
Comments: Population: Caucasian.

Proper citation: Coriell Cat# GM13267, RRID:CVCL_4F67 Copy   


  • RRID:CVCL_AX25

https://web.expasy.org/cellosaurus/CVCL_AX25

Organism: Homo sapiens (Human)
Disease: Niemann-Pick disease, type A
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_AX25 Copy   



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