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Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in EuropeFrontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology.Characterizing facial features in individuals with craniofacial microsomia: A systematic approach for clinical research.A Diagnostic Conundrum: Ectopic Nasal Ossification, Submucosal Alveolar Cleft, Absent Posterior Atlantal Arch, and Corpus Callosum Lipoma.Oculoauriculofrontonasal Dysplasia Syndrome With Additional Clinical Features.Oculoauriculofrontonasal syndrome: Case series revealing new bony nasal anomalies in an old syndrome
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on April 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Characterizing the oculoauriculofrontonasal syndrome.
@en
Characterizing the oculoauriculofrontonasal syndrome.
@nl
type
label
Characterizing the oculoauriculofrontonasal syndrome.
@en
Characterizing the oculoauriculofrontonasal syndrome.
@nl
prefLabel
Characterizing the oculoauriculofrontonasal syndrome.
@en
Characterizing the oculoauriculofrontonasal syndrome.
@nl
P2093
P50
P1476
Characterizing the oculoauriculofrontonasal syndrome
@en
P2093
Marjan M Nezarati
Rani Sachdev
Salim Aftimos
P356
10.1097/MCD.0B013E3282F449C8
P577
2008-04-01T00:00:00Z