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On page 9 showing 161 ~ 180 out of 205 results
Snippet view Table view Download 205 Result(s)
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  • RRID:CVCL_9Q34

https://web.expasy.org/cellosaurus/CVCL_9Q34

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_9Q34 Copy   


  • RRID:CVCL_9M23

https://web.expasy.org/cellosaurus/CVCL_9M23

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 47,XXY,t(3;4)(q26.32;q31.1)mat (ECACC=98032405)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 98032405, RRID:CVCL_9M23 Copy   


  • RRID:CVCL_9F76

https://web.expasy.org/cellosaurus/CVCL_9F76

Organism: Homo sapiens (Human)
Disease: 47,XYY syndrome
Category: Finite cell line
Comments: Karyotypic information: 47,XYY (ECACC=93080202)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 93080202, RRID:CVCL_9F76 Copy   


  • RRID:CVCL_9H13

https://web.expasy.org/cellosaurus/CVCL_9H13

Organism: Homo sapiens (Human)
Disease: Congenital cystic hygroma
Category: Finite cell line
Comments: Karyotypic information: 69,XXX (ECACC=94011410)., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_9H13 Copy   


  • RRID:CVCL_9H71

https://web.expasy.org/cellosaurus/CVCL_9H71

Organism: Homo sapiens (Human)
Disease: True hermaphroditism
Category: Finite cell line
Comments: Karyotypic information: 46,XX (ECACC=94032807)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 94032807, RRID:CVCL_9H71 Copy   


  • RRID:CVCL_9H70

https://web.expasy.org/cellosaurus/CVCL_9H70

Organism: Homo sapiens (Human)
Disease: True hermaphroditism
Category: Finite cell line
Comments: Karyotypic information: 46,XX (ECACC=94032502)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 94032502, RRID:CVCL_9H70 Copy   


  • RRID:CVCL_9H71

https://web.expasy.org/cellosaurus/CVCL_9H71

Organism: Homo sapiens (Human)
Disease: True hermaphroditism
Category: Finite cell line
Comments: Karyotypic information: 46,XX (ECACC=94032807)., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_9H71 Copy   


  • RRID:CVCL_LC40

Possibly Discontinued

https://web.expasy.org/cellosaurus/CVCL_LC40

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments:

Proper citation: JCRB Cat# JCRB3045, RRID:CVCL_LC40 Copy   


  • RRID:CVCL_B3MD

https://web.expasy.org/cellosaurus/CVCL_B3MD

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments:

Proper citation: JCRB Cat# JCRB3069, RRID:CVCL_B3MD Copy   


  • RRID:CVCL_B3MD

https://web.expasy.org/cellosaurus/CVCL_B3MD

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_B3MD Copy   


  • RRID:CVCL_B3ME

https://web.expasy.org/cellosaurus/CVCL_B3ME

Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments:

Proper citation: RRID:CVCL_B3ME Copy   


  • RRID:CVCL_8W84

https://web.expasy.org/cellosaurus/CVCL_8W84

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_8W84 Copy   


  • RRID:CVCL_8W84

https://web.expasy.org/cellosaurus/CVCL_8W84

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 89030291, RRID:CVCL_8W84 Copy   


  • RRID:CVCL_8X30

https://web.expasy.org/cellosaurus/CVCL_8X30

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Asian., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_8X30 Copy   


  • RRID:CVCL_8X31

https://web.expasy.org/cellosaurus/CVCL_8X31

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_8X31 Copy   


  • RRID:CVCL_8Y18

https://web.expasy.org/cellosaurus/CVCL_8Y18

Organism: Homo sapiens (Human)
Disease: Russell-Silver syndrome
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.

Proper citation: RRID:CVCL_8Y18 Copy   


  • RRID:CVCL_8Y18

https://web.expasy.org/cellosaurus/CVCL_8Y18

Organism: Homo sapiens (Human)
Disease: Russell-Silver syndrome
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 00102801, RRID:CVCL_8Y18 Copy   


  • RRID:CVCL_B542

https://web.expasy.org/cellosaurus/CVCL_B542

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments: From: Reproductive Genetics Institute; Chicago; USA.

Proper citation: RRID:CVCL_B542 Copy   


  • RRID:CVCL_B688

https://web.expasy.org/cellosaurus/CVCL_B688

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments: From: Reproductive Genetics Institute; Chicago; USA.

Proper citation: RRID:CVCL_B688 Copy   


  • RRID:CVCL_C358

https://web.expasy.org/cellosaurus/CVCL_C358

Organism: Homo sapiens (Human)
Disease:
Category: Embryonic stem cell
Comments: From: University of Edinburgh; Edinburgh; United Kingdom.

Proper citation: RRID:CVCL_C358 Copy   



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