l9n/ New Jersey

2014–2015 Session

Senate Bill 2400

Establishes central registry for sickle cell trait diagnoses; provides for informational outreach and genetic counseling.

Did not become law. It stopped in the Senate's Budget and Appropriations Committee on March 12, 2015. The 2014–2015 session has ended.

Sponsors

Who carried the bill in each chamber, and who signed on. Each name leads to the member's page.

In the Senate

1 co-sponsor

Shirley K. Turner

Its course

September 18, 2014 to March 12, 2015, on one scale. In the top row each mark is a day something happened; taller marks are busier days.

Each committee stop sits inside its chamber.

Every action3 actions on 3 days

In the SenateSep 18 to Mar 12 · stopped175 days

Budget and AppropriationsMar 12 to Mar 12 · stopped0 days

Text

Each version as the Legislature printed it.

l9n doesn't hold this bill's text yet.

What happened

In l9n's words, one line for each step. Every action as the Legislature published it is below.

In the Senate Sep 18 – Mar 12, 2015

  1. Introduced in the Senate and sent to Health, Human Services and Senior Citizens
  2. Health, Human Services and Senior Citizens recommended it
  3. Read a second time
  4. Sent to Budget and Appropriations
All 3 actions, as published