| No. Panggil : | Human Molecular Genetics: Volume 22, Issue 7: 1 April 2013: p. 1358-1372 |
| Judul : | Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel?Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects |
| Pengarang : | |
| Penerbit dan Distribusi : | United Kingdom : Oxford University Press, 2013 |
| Subjek : | |
| Jenis Bahan : | {007/00} |
| Lokasi : |
| Nomor Panggil | No. Barkod | Ketersediaan |
|---|---|---|
| Human Molecular Genetics: Volume 22, Issue 7: 1 April 2013: p. 1358-1372 | Human Molecular Genetics: Volume 22, Issue 7: 1 April 2013: p. 1358-1372 | TERSEDIA |
| Ulasan Anggota: |
| Tidak ada ulasan pada koleksi ini: 73391 |
