Hasil Pencarian - Renata Gallagher

  • Menampilkan 1 - 2 hasil dari 2
Perbaiki Hasil
  1. 1
    A case of severe acidosis in a 12-month-old: Succinyl-CoA:3-ketoacidCoA transferase deficiency with gene mutations

    A case of severe acidosis in a 12-month-old: Succinyl-CoA:3-ketoacidCoA transferase deficiency with gene mutations oleh Navjot Dhammi, Jenna Essakow, Renata Gallagher, Cynthia Gaw

    Diterbitkan 2022-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    Genomic Analysis of Historical Cases with Positive Newborn Screens for Short-Chain Acyl-CoA Dehydrogenase Deficiency Shows That a Validated Second-Tier Biochemical Test Can Replace Future Sequencing

    Genomic Analysis of Historical Cases with Positive Newborn Screens for Short-Chain Acyl-CoA Dehydrogenase Deficiency Shows That a Validated Second-Tier Biochemical Test Can Replace... oleh Aashish N. Adhikari, Robert J. Currier, Hao Tang, Coleman T. Turgeon, Robert L. Nussbaum, Rajgopal Srinivasan, Uma Sunderam, Pui-Yan Kwok, Steven E. Brenner, Dimitar Gavrilov, Jennifer M. Puck, Renata Gallagher

    Diterbitkan 2020-05-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: