| dc.contributor.author | Dogan, DG | |
| dc.contributor.author | Dogan, M | |
| dc.contributor.author | Aslan, M | |
| dc.contributor.author | Menekse, E | |
| dc.contributor.author | Yakinci, C | |
| dc.date.accessioned | 2022-03-28T11:41:35Z | |
| dc.date.available | 2022-03-28T11:41:35Z | |
| dc.date.issued | 2010 | |
| dc.identifier.uri | http://hdl.handle.net/11616/58037 | |
| dc.description.abstract | Hanhart syndrome: We report on a male infant with Hanhart Syndrome. It is classified in "oromandibular limb hypogenesis syndromes" which are a group of rare conditions involving congenital malformations of tongue, mandible, and limbs. | |
| dc.source | GENETIC COUNSELING | |
| dc.title | HANHART SYNDROME |
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