|
|||||
|
|
Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotype |
|
| Authors: | Ellen Markljung Tatjana Adamovic Jia Cao Hussein Naji Sylvie Kaiser Tomas Wester Agneta Nordenskjöld |
| Institution: | Department of Women's and Children's Health and Center for Molecular Medicine CMM02, Karolinska Institutet, SE-171 76 Stockholm, Sweden. |
| Abstract: | |
| Keywords: | CS Currarino syndrome CT Computed Tomography HB9 Homeobox 9 HCG Human chorionic gonadotropin HLXB9 Homeobox gene HB9 MNX1 Motor neuron and pancreas homeobox-1 MRI Magnetic resonance imaging |
| 本文献已被 ScienceDirect PubMed 等数据库收录！ | |