Results 171 to 180 of about 6,877 (203)
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Orthodontics & Craniofacial Research, 2007
Structured AbstractAuthors – Dixon J, Trainor P, Dixon MJTreacher Collins syndrome (TCS) is an autosomal dominant disorder of craniofacial development which results from loss‐of‐function mutations in the gene TCOF1. TCOF1 encodes the nucleolar phosphoprotein, Treacle, which plays a key role in pre‐ribosomal processing and ribosomal biogenesis. In mice,
Dixon, Jill +2 more
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Structured AbstractAuthors – Dixon J, Trainor P, Dixon MJTreacher Collins syndrome (TCS) is an autosomal dominant disorder of craniofacial development which results from loss‐of‐function mutations in the gene TCOF1. TCOF1 encodes the nucleolar phosphoprotein, Treacle, which plays a key role in pre‐ribosomal processing and ribosomal biogenesis. In mice,
Dixon, Jill +2 more
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Archives of Otolaryngology - Head and Neck Surgery, 1964
Although the Treacher-Collins syndrome is not a new entity and cases have been reported sporadically since Berry in 1888 first reported two cases of congenital coloboma of the lower eyelids, it is surprising that little has been written concerning the otologic aspects of this very interesting, if unfortunate, aggregate of congenital malformations.
A O, FERNANDEZ, M L, RONIS
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Although the Treacher-Collins syndrome is not a new entity and cases have been reported sporadically since Berry in 1888 first reported two cases of congenital coloboma of the lower eyelids, it is surprising that little has been written concerning the otologic aspects of this very interesting, if unfortunate, aggregate of congenital malformations.
A O, FERNANDEZ, M L, RONIS
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Clinics in Plastic Surgery, 2019
Treacher Collins syndrome is a rare genetic disorder of craniofacial development with a highly variable phenotype. The disorder displays an intricate underlying dysmorphology. Affected patients may suffer life-threatening airway complications and functional difficulties involving sight, hearing, speech, and feeding.
Albaraa, Aljerian, Mirko S, Gilardino
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Treacher Collins syndrome is a rare genetic disorder of craniofacial development with a highly variable phenotype. The disorder displays an intricate underlying dysmorphology. Affected patients may suffer life-threatening airway complications and functional difficulties involving sight, hearing, speech, and feeding.
Albaraa, Aljerian, Mirko S, Gilardino
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Familial Treacher-Collins syndrome
The Journal of Laryngology & Otology, 1988The major congenital malformations of the first and second branchial arch derivatives such as mandibulofacial dysostosis have a genetic basis. Treacher-Collins syndrome is transmitted as an autosomal dominant trait, although many cases occur as spontaneous mutations.
P S, Murty +3 more
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The British Journal of Radiology, 1954
The main clinical and radiological features of two cases of Treacher Collins syndrome have been described. Radiologically, the outstanding features are: (1) Agenesis of the malar bones. (a) Non-fusion of the zygomatic arches. (b) Absence of the bodies of the malar bones.
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The main clinical and radiological features of two cases of Treacher Collins syndrome have been described. Radiologically, the outstanding features are: (1) Agenesis of the malar bones. (a) Non-fusion of the zygomatic arches. (b) Absence of the bodies of the malar bones.
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Costi D, Endlich Y: Treacher-Collins syndrome, 2022
null Gayathri Sreedher, MBBS, MD +1 more
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null Gayathri Sreedher, MBBS, MD +1 more
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2021
The aim of this bachelor thesis is to provide the general public with awareness of the Treacher Collins syndrome. Learn what specificities such people get and what difficulties are associated with this syndrome. Furthermore, to point out possible problems in the adoption of the child by the family and its gradual adaptation. The practical part consists
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The aim of this bachelor thesis is to provide the general public with awareness of the Treacher Collins syndrome. Learn what specificities such people get and what difficulties are associated with this syndrome. Furthermore, to point out possible problems in the adoption of the child by the family and its gradual adaptation. The practical part consists
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Determination of the Collins-Soper Kernel from Lattice QCD
Journal of High Energy Physics, 2021Alexey A Vladimirov +2 more
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