| Hanhart syndrome. | |
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MedLine Citation:
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PMID: 21290964 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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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. |
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Authors:
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D G Dogan; M Dogan; M Aslan; E Menekse; C Yakinci |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Genetic counseling (Geneva, Switzerland) Volume: 21 ISSN: 1015-8146 ISO Abbreviation: Genet. Couns. Publication Date: 2010 |
Date Detail:
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Created Date: 2011-02-04 Completed Date: 2011-03-02 Revised Date: 2011-12-06 |
Medline Journal Info:
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Nlm Unique ID: 9015261 Medline TA: Genet Couns Country: Switzerland |
Other Details:
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Languages: eng Pagination: 359-62 Citation Subset: IM |
Affiliation:
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Department of Pediatrics, Inönü University, Faculty of Medicine, Turgut Ozal Medical Center, Malatya, Turkey. deryagumus@yahoo.com |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple*
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radiography Craniofacial Abnormalities* / radiography Fatal Outcome Humans Infant, Newborn Limb Deformities, Congenital* / radiography Male Tongue / abnormalities |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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