Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotype |
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Authors: | Ellen Markljung Tatjana Adamovic Jia Cao Hussein Naji Sylvie Kaiser Tomas Wester Agneta Nordenskjöld |
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Affiliation: | Department of Women's and Children's Health and Center for Molecular Medicine CMM02, Karolinska Institutet, SE-171 76 Stockholm, Sweden. |
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Abstract: | |
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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 |
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