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On page 168 showing 3341 ~ 3360 out of 117,735 results
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  • RRID:CVCL_5N72

https://web.expasy.org/cellosaurus/CVCL_5N72

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line

Proper citation: Coriell Cat# GM07939, RRID:CVCL_5N72 Copy   


  • RRID:CVCL_2T37

https://web.expasy.org/cellosaurus/CVCL_2T37

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

Proper citation: Coriell Cat# GM07891, RRID:CVCL_2T37 Copy   


  • RRID:CVCL_4H45

https://web.expasy.org/cellosaurus/CVCL_4H45

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection.

Proper citation: RRID:CVCL_4H45 Copy   


  • RRID:CVCL_2T43

https://web.expasy.org/cellosaurus/CVCL_2T43

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

Proper citation: RRID:CVCL_2T43 Copy   


  • RRID:CVCL_2T44

https://web.expasy.org/cellosaurus/CVCL_2T44

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

Proper citation: Coriell Cat# GM07994, RRID:CVCL_2T44 Copy   


  • RRID:CVCL_5N71

https://web.expasy.org/cellosaurus/CVCL_5N71

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

Proper citation: RRID:CVCL_5N71 Copy   


  • RRID:CVCL_4F94

https://web.expasy.org/cellosaurus/CVCL_4F94

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

Proper citation: Coriell Cat# GM07924, RRID:CVCL_4F94 Copy   


  • RRID:CVCL_AT08

https://web.expasy.org/cellosaurus/CVCL_AT08

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY,9qh- (Coriell=GM08147)., Population: Caucasian.

Proper citation: RRID:CVCL_AT08 Copy   


  • RRID:CVCL_2T46

https://web.expasy.org/cellosaurus/CVCL_2T46

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

Proper citation: RRID:CVCL_2T46 Copy   


  • RRID:CVCL_2T49

https://web.expasy.org/cellosaurus/CVCL_2T49

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

Proper citation: RRID:CVCL_2T49 Copy   


  • RRID:CVCL_5M41

https://web.expasy.org/cellosaurus/CVCL_5M41

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

Proper citation: RRID:CVCL_5M41 Copy   


  • RRID:CVCL_2T47

https://web.expasy.org/cellosaurus/CVCL_2T47

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

Proper citation: Coriell Cat# GM08070, RRID:CVCL_2T47 Copy   


  • RRID:CVCL_5M39

https://web.expasy.org/cellosaurus/CVCL_5M39

Organism: Homo sapiens (Human)
Disease: Fanconi anemia
Category: Transformed cell line

Proper citation: Coriell Cat# GM08010, RRID:CVCL_5M39 Copy   


  • RRID:CVCL_5M39

https://web.expasy.org/cellosaurus/CVCL_5M39

Organism: Homo sapiens (Human)
Disease: Fanconi anemia
Category: Transformed cell line

Proper citation: RRID:CVCL_5M39 Copy   


  • RRID:CVCL_AI43

https://web.expasy.org/cellosaurus/CVCL_AI43

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.

Proper citation: Coriell Cat# GM08071, RRID:CVCL_AI43 Copy   


  • RRID:CVCL_N076

https://web.expasy.org/cellosaurus/CVCL_N076

Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.

Proper citation: RRID:CVCL_N076 Copy   


  • RRID:CVCL_2T47

https://web.expasy.org/cellosaurus/CVCL_2T47

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

Proper citation: RRID:CVCL_2T47 Copy   


  • RRID:CVCL_N075

https://web.expasy.org/cellosaurus/CVCL_N075

Organism: Homo sapiens (Human)
Disease: HMG-CoA lyase deficiency
Category: Finite cell line
Comments: Population: Egyptian.

Proper citation: Coriell Cat# GM08100, RRID:CVCL_N075 Copy   


  • RRID:CVCL_1N82

https://web.expasy.org/cellosaurus/CVCL_1N82

Organism: Homo sapiens (Human)
Disease: Beckwith-Wiedemann syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY.arr(1-22)x2,(XY)x1 (Coriell=GM08206)., Population: Caucasian.

Proper citation: RRID:CVCL_1N82 Copy   


  • RRID:CVCL_AT08

https://web.expasy.org/cellosaurus/CVCL_AT08

Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY,9qh- (Coriell=GM08147)., Population: Caucasian.

Proper citation: Coriell Cat# GM08147, RRID:CVCL_AT08 Copy   



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