Síndrome de Jacobsen (deleción 11q): a propósito de un caso
Jacobsen syndrome is an uncommon chromosomopathy, caused by a terminal deletion of the long arm of chromosome 11. The main clinical features are psychomotor and growth retardation, trigonocephaly and characteristic facial dysmorphism, but there are many associated alterations. The craniofacial dysm...
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| Main Authors: | , , , , |
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| Format: | Article |
| Language: | Spanish |
| Published: |
2020
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| Subjects: | |
| Online Access: | https://dialnet.unirioja.es/servlet/oaiart?codigo=7752629 |
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