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On page 208 showing 4141 ~ 4160 out of 6,967 results
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  • RRID:CVCL_9F24

https://web.expasy.org/cellosaurus/CVCL_9F24

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

Proper citation: ECACC Cat# 93050703, RRID:CVCL_9F24 Copy   


  • RRID:CVCL_9F37

https://web.expasy.org/cellosaurus/CVCL_9F37

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

Proper citation: ECACC Cat# 93060324, RRID:CVCL_9F37 Copy   


  • RRID:CVCL_9F44

https://web.expasy.org/cellosaurus/CVCL_9F44

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX; 47,XX,+mar(9)mat (ECACC=93061517)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 93061517, RRID:CVCL_9F44 Copy   


  • RRID:CVCL_9F01

https://web.expasy.org/cellosaurus/CVCL_9F01

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

Proper citation: ECACC Cat# 93040827, RRID:CVCL_9F01 Copy   


  • RRID:CVCL_9F08

https://web.expasy.org/cellosaurus/CVCL_9F08

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX; 47,XX+mar(15); de novo (ECACC=93042102)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 93042102, RRID:CVCL_9F08 Copy   


  • RRID:CVCL_9F02

https://web.expasy.org/cellosaurus/CVCL_9F02

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,t(5;15)(q13.1;q21.1)pat (ECACC=93040828)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 93040828, RRID:CVCL_9F02 Copy   


  • RRID:CVCL_9F15

https://web.expasy.org/cellosaurus/CVCL_9F15

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 47,XX,+mar(14) (ECACC=93042302)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 93042302, RRID:CVCL_9F15 Copy   


  • RRID:CVCL_9F10

https://web.expasy.org/cellosaurus/CVCL_9F10

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

Proper citation: ECACC Cat# 93042108, RRID:CVCL_9F10 Copy   


  • RRID:CVCL_9E96

https://web.expasy.org/cellosaurus/CVCL_9E96

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

Proper citation: ECACC Cat# 93040805, RRID:CVCL_9E96 Copy   


  • RRID:CVCL_9F89

https://web.expasy.org/cellosaurus/CVCL_9F89

Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 93082012, RRID:CVCL_9F89 Copy   


  • RRID:CVCL_9F69

https://web.expasy.org/cellosaurus/CVCL_9F69

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,t(7;16)(p15;q22) (ECACC=93071611)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 93071611, RRID:CVCL_9F69 Copy   


  • RRID:CVCL_9F53

https://web.expasy.org/cellosaurus/CVCL_9F53

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX [9]; 47,XX,+mar(9) [21] (ECACC=93062901)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 93062901, RRID:CVCL_9F53 Copy   


  • RRID:CVCL_9F48

https://web.expasy.org/cellosaurus/CVCL_9F48

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

Proper citation: ECACC Cat# 93061522, RRID:CVCL_9F48 Copy   


  • RRID:CVCL_9F50

https://web.expasy.org/cellosaurus/CVCL_9F50

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,var(20p)(?0) (ECACC=93061809)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 93061809, RRID:CVCL_9F50 Copy   


  • RRID:CVCL_9F59

https://web.expasy.org/cellosaurus/CVCL_9F59

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XY [8]; 47,XY,+8 [22] (ECACC=93070821)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 93070821, RRID:CVCL_9F59 Copy   


  • RRID:CVCL_9F45

https://web.expasy.org/cellosaurus/CVCL_9F45

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

Proper citation: ECACC Cat# 93061518, RRID:CVCL_9F45 Copy   


  • RRID:CVCL_9F61

https://web.expasy.org/cellosaurus/CVCL_9F61

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,t(2;10)(p21;p15)(?0) (ECACC=93070823)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 93070823, RRID:CVCL_9F61 Copy   


  • RRID:CVCL_9F57

https://web.expasy.org/cellosaurus/CVCL_9F57

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,t(5;6)(q22;q13) (ECACC=93063007)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 93063007, RRID:CVCL_9F57 Copy   


  • RRID:CVCL_9F51

https://web.expasy.org/cellosaurus/CVCL_9F51

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

Proper citation: ECACC Cat# 93062503, RRID:CVCL_9F51 Copy   


  • RRID:CVCL_9F85

https://web.expasy.org/cellosaurus/CVCL_9F85

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

Proper citation: ECACC Cat# 93081711, RRID:CVCL_9F85 Copy   



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