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On page 222 showing 4421 ~ 4440 out of 6,967 results
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  • RRID:CVCL_9D42

https://web.expasy.org/cellosaurus/CVCL_9D42

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,inv(13)(q33.2;q34)mat (ECACC=92101503)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 92101503, RRID:CVCL_9D42 Copy   


  • RRID:CVCL_AQ61

https://web.expasy.org/cellosaurus/CVCL_AQ61

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

Proper citation: ECACC Cat# 92081809, RRID:CVCL_AQ61 Copy   


  • RRID:CVCL_9D41

https://web.expasy.org/cellosaurus/CVCL_9D41

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

Proper citation: ECACC Cat# 92101502, RRID:CVCL_9D41 Copy   


  • RRID:CVCL_9D14

https://web.expasy.org/cellosaurus/CVCL_9D14

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

Proper citation: ECACC Cat# 92082110, RRID:CVCL_9D14 Copy   


  • RRID:CVCL_9D52

https://web.expasy.org/cellosaurus/CVCL_9D52

Organism: Homo sapiens (Human)
Disease: Familial adenomatous polyposis
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,rec(5)del(q15;q22),ins(5)(q22.3;q14.2;q15)mat (ECACC=92102902)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 92102902, RRID:CVCL_9D52 Copy   


  • RRID:CVCL_9D23

https://web.expasy.org/cellosaurus/CVCL_9D23

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,del(2)(pter->q37.1); de novo (ECACC=92091002)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 92091002, RRID:CVCL_9D23 Copy   


  • RRID:CVCL_9D25

https://web.expasy.org/cellosaurus/CVCL_9D25

Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,t(3;20)(q13.2;p12.2); de novo (ECACC=92091006)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 92091006, RRID:CVCL_9D25 Copy   


  • RRID:CVCL_9D49

https://web.expasy.org/cellosaurus/CVCL_9D49

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

Proper citation: ECACC Cat# 92102361, RRID:CVCL_9D49 Copy   


  • RRID:CVCL_9D06

https://web.expasy.org/cellosaurus/CVCL_9D06

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

Proper citation: ECACC Cat# 92081429, RRID:CVCL_9D06 Copy   


  • RRID:CVCL_9D08

https://web.expasy.org/cellosaurus/CVCL_9D08

Organism: Homo sapiens (Human)
Disease: Klinefelter syndrome
Category: Finite cell line
Comments: Karyotypic information: 47,XXY (ECACC=92081433)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 92081433, RRID:CVCL_9D08 Copy   


  • RRID:CVCL_9D21

https://web.expasy.org/cellosaurus/CVCL_9D21

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

Proper citation: ECACC Cat# 92090805, RRID:CVCL_9D21 Copy   


  • RRID:CVCL_9D05

https://web.expasy.org/cellosaurus/CVCL_9D05

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX; 46,X,r(X) (ECACC=92081102)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 92081102, RRID:CVCL_9D05 Copy   


  • RRID:CVCL_9D35

https://web.expasy.org/cellosaurus/CVCL_9D35

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

Proper citation: ECACC Cat# 92092902, RRID:CVCL_9D35 Copy   


  • RRID:CVCL_9I31

https://web.expasy.org/cellosaurus/CVCL_9I31

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

Proper citation: ECACC Cat# 94071514, RRID:CVCL_9I31 Copy   


  • RRID:CVCL_9I45

https://web.expasy.org/cellosaurus/CVCL_9I45

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,-5,+der(5),t(5;11)(p15;p15)pat (ECACC=94080811)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 94080811, RRID:CVCL_9I45 Copy   


  • RRID:CVCL_9I43

https://web.expasy.org/cellosaurus/CVCL_9I43

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

Proper citation: ECACC Cat# 94080523, RRID:CVCL_9I43 Copy   


  • RRID:CVCL_9I62

https://web.expasy.org/cellosaurus/CVCL_9I62

Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+18 (ECACC=94083002)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 94083002, RRID:CVCL_9I62 Copy   


  • RRID:CVCL_9I65

https://web.expasy.org/cellosaurus/CVCL_9I65

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

Proper citation: ECACC Cat# 94083106, RRID:CVCL_9I65 Copy   


  • RRID:CVCL_9I71

https://web.expasy.org/cellosaurus/CVCL_9I71

Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(1;3)(q21;q25)pat (ECACC=94090717)., Part of: ECACC chromosomal abnormality collection.

Proper citation: ECACC Cat# 94090717, RRID:CVCL_9I71 Copy   


  • RRID:CVCL_9I54

https://web.expasy.org/cellosaurus/CVCL_9I54

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

Proper citation: ECACC Cat# 94081610, RRID:CVCL_9I54 Copy   



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