l9n/ New Jersey

2014–2015 Session

Assembly Bill 3356

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 December 7, 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 General Assembly

7 co-sponsors

Angel Fuentes, Shavonda E. Sumter, Elizabeth Maher Muoio, L. Grace Spencer, Nancy J. Pinkin, Mila M. Jasey, Cleopatra G. Tucker

Its course

June 5, 2014 to December 7, 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 action5 actions on 4 days

In the General AssemblyJun 5 to Dec 3546 days

Health and Senior ServicesJun 5 to Jun 50 days

AppropriationsJun 5 to Nov 9522 days

In the SenateDec 3 to Dec 7 · stopped4 days

Budget and AppropriationsDec 7 to Dec 7 · stopped0 days

Votes

Yeas to nays, as the Legislature recorded them. Committee votes are set in.

  • General Assembly, third reading50–3

    Passed · Dec 3, 2015 · 9 present

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 General Assembly Jun 5 – Dec 3, 2015

  1. Introduced in the General Assembly and sent to Health and Senior Services
  2. Health and Senior Services recommended it
  3. Sent to Appropriations
  4. Appropriations recommended it
  5. Read a second time
  6. Passed the General Assembly, 50 to 3

In the Senate Dec 7, 2015

  1. Arrived in the Senate
  2. Sent to Budget and Appropriations
All 5 actions, as published