SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature.
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Solitary median maxillary central incisor (SMMCI) syndromeSonic hedgehog is essential for first pharyngeal arch developmentHedgehog signaling is required at multiple stages of zebrafish tooth developmentCT and MRI of congenital nasal lesions in syndromic conditions.Single median maxillary central incisor: new data and mutation review.Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly.The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes.Expression of SHH signaling molecules in the developing human primary dentitionMultiple hits during early embryonic development: digenic diseases and holoprosencephalyTowards a new classification of ectodermal dysplasias.Hedgehog signaling regulates dental papilla formation and tooth size during zebrafish odontogenesis.Utilizing prospective sequence analysis of SHH, ZIC2, SIX3 and TGIF in holoprosencephaly probands to describe the parameters limiting the observed frequency of mutant gene×gene interactionsTwo patients with small chromosome 22q11.21 alterations and central nervous system abnormalities.Functional characterization of a heterozygous GLI2 missense mutation in patients with multiple pituitary hormone deficiency.Congenital nasal pyriform aperture stenosis in association with solitary median maxillary central incisor: unique radiologic features.Developmental disorders of the dentition: an update.The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.Current knowledge of tooth development: patterning and mineralization of the murine dentition.Solitary median maxillary central incisor in association with hemifacial microsomia: A rare case report and review of literature.Sella turcica morphology and the pituitary gland-a new contribution to craniofacial diagnostics based on histology and neuroradiology.A new syndrome with overlapping features of Townes-brocks syndrome and single median maxillary central incisor syndrome.Solitary median maxillary central incisor syndrome (SMMCI) with congenital nasal puriform aperture stenosis: literature review and case report with comprehensive dental treatment and 14 years follow-up.Bardet-Biedl syndrome 3 regulates the development of cranial base midline structuresSonic hedgehog gene-enhanced tissue engineering for bone regeneration.Functional characterization of sonic hedgehog mutations associated with holoprosencephaly.Molecular mechanisms of OLIG2 transcription factor in brain cancer.Clinical course and implications of congenital nasal pyriform stenosis and solitary median maxillary central incisor in a newborn: a case report.Dental approach to craniofacial syndromes: how can developmental fields show us a new way to understand pathogenesis?Sonic hedgehog.Sonic hedgehog mutations identified in holoprosencephaly patients can act in a dominant negative manner.Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the Sonic Hedgehog gene and the HLXB9 gene at 7q36.3.The neurocranial and craniofacial morphology in children with solitary median maxillary central incisor (SMMCI).Genotypic and phenotypic variation in six patients with solitary median maxillary central incisor syndrome.The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis.Maternally inherited heterozygous sequence change in the sonic hedgehog gene in a male patient with bilateral closed-lip schizencephaly and partial absence of the corpus callosum.
P2860
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P2860
SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature.
description
2001 nî lūn-bûn
@nan
2001 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
SHH mutation is associated wit ...... and review of the literature.
@ast
SHH mutation is associated wit ...... and review of the literature.
@en
SHH mutation is associated wit ...... and review of the literature.
@nl
type
label
SHH mutation is associated wit ...... and review of the literature.
@ast
SHH mutation is associated wit ...... and review of the literature.
@en
SHH mutation is associated wit ...... and review of the literature.
@nl
prefLabel
SHH mutation is associated wit ...... and review of the literature.
@ast
SHH mutation is associated wit ...... and review of the literature.
@en
SHH mutation is associated wit ...... and review of the literature.
@nl
P2093
P2860
P1476
SHH mutation is associated wit ...... and review of the literature.
@en
P2093
P2860
P356
10.1002/1096-8628(20010722)102:1<1::AID-AJMG1336>3.0.CO;2-U
P577
2001-07-01T00:00:00Z