Oromandibular limb hypogenesis complex (Hanhart syndrome): A severe adult phenotype
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference17 articles.
1. Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome
2. Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome ?A pathogenetic hypothesis
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4. A mutational analysis of the 5′ HoxD genes: dissection of genetic interactions during limb development in the mouse
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1. Acromelia-oligodontia syndrome;Clinical Case Reports;2017-05-05
2. Hypoglossia-Hypodactylia Syndrome;Atlas of Genetic Diagnosis and Counseling;2017
3. Hypoglossia-Hypodactylia Syndrome;Atlas of Genetic Diagnosis and Counseling;2016
4. Hypoglossia-Hypodactyly Syndrome with Short Stature - A Case Report;J CLIN DIAGN RES;2014
5. Modification of Mandibular Advancement Osteotomy in a Patient With Hanhart Syndrome;Journal of Craniofacial Surgery;2013-11
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