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JJ Fresno Mall Front Bumper Cover Compatible 1992-1995 Civic CX with Max 57% OFF 1992-19

JJ Front Bumper Cover Compatible with 1992-1995 Civic CX 1992-19

$150

JJ Front Bumper Cover Compatible with 1992-1995 Civic CX 1992-19

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Product description

Front Bumper Cover For 1992-1995 Civic Coupe and Hatchback 71101SR0A00ZZ:

Description:
Warranty: 1 Year
Warranty Terms and Conditions
Terms of Use
Warranty Cover age Policy

Replacement Bumper Cover 1367P:
Manufactured from top quality components, this is your best option and inexpensive replacement for your rebuild, Repair , and maintenance needs - an OE replacement product for your damaged or aged factory part.
Replacement - the most affordable brand name for replacement parts that you need! Replacement is a professional brand for autobody, lighting parts, electrical, brake, suspension, intake and exhaust, and cooling and heating products. All Replacement brands include 1-year, unlimited-mileage warranty.

Notes:
Location : Front
Brand New in the Box - Fit and Quality Guaranteed!

Material: Plastic
Quantity sold: Sold individually
Product fit: Direct Fit
Replaces oe number: 71101SR0A00ZZ
Color/finish: Primed
Recommended use: OE Replacement
Replaces partslink number: HO1000141
License plate provision: With license plate provision
Receiver and tow hook hole: Without tow hook hole
Notes: With spoiler holes
Fog light holes: Without Fog Light Holes
Parking aid sensor holes: Without parking aid sensor holes
Interchange part number: 71101SR0A00ZZ, HO1000141
Condition: New
Location: Front

Compatible with the following vehicles::

:
92 Civic DX For Hatchback Models
92-95 Civic (submodel: CX, Si, VX) For Hatchback Models
93-95 Civic (submodel: DX, EX) For Coupe or Hatchback

JJ Front Bumper Cover Compatible with 1992-1995 Civic CX 1992-19

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Barrett’s oesophagus may be the precursor of all oesophageal adenocarcinomas

To cite: Curtius K, Rubenstein JH, Chak A, et al. Gut 2021;70:1435-1440.

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Objective: Barrett’s oesophagus (BE) is a known precursor to oesophageal adenocarcinoma (OAC) but current clinical data have not been consolidated to address whether BE is the origin of all incident OAC, which would reinforce evidence for BE screening efforts. We aimed to answer whether all expected prevalent BE, diagnosed and undiagnosed, could account for all incident OACs in the US cancer registry data.

Conclusion: There are likely few additional OAC cases arising in the US population outside those expected from individuals with BE. Effective screening of high-risk patients could capture the majority of population destined for OAC progression and potentially decrease mortality through early detection and curative removal of small (pre)cancers during surveillance.

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