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Results for
""Tooth Abnormalities""[mesh_terms]

9 Results

Searching titles within these results

Third case of cerebral, ocular, dental, auricular, skeletal anomalies (CODAS) syndrome, further delineating a new malformation syndrome: first report of an affected male and review of literature.

A M Innes, A E Chudley, M H Reed, E P Shuckett, G E Hildes-Ripstein, C R Greenberg

American journal of medical genetics 2001;102(1):44-7

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Smith-Lemli-Opitz syndrome: a review, case report and dental implications.

Kathleen B Muzzin, Lisa F Harper

Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry 2003;23(1):22-7

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Oral and craniofacial findings in a patient with methylmalonic aciduria and homocystinuria: review and a case report.

G D'Alessandro, T Tagariello, G Piana

Minerva stomatologica 2010;59(3):129-37

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Two novel GJA1 variants in oculodentodigital dysplasia.

Nikolai P Pace, Valerie Benoit, David Agius, Maria Angela Grima, Raymond Parascandalo, Pascale Hilbert, Isabella Borg

Molecular genetics & genomic medicine 2020;7(9):e882

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Novel ocular findings in oculodentodigital dysplasia (ODDD): a case report and literature review.

Limei Sun, Panfeng Wang, Chonglin Chen, Aiyuan Zhang, Weiqing Wang, Xiaoyan Ding, Zhirong Wang

Ophthalmic genetics 2020;40(1):54-59

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Rare Germline Variants in the Adenomatous Polyposis Coli Gene Associated with Dental and Osseous Anomalies.

Judit Bene, Gergely Büki, Gréta Antal

International journal of molecular sciences 2024;25(15):

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Ion channels, channelopathies, and tooth formation.

X Duan

Journal of dental research 2014;93(2):117-25

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Identification of a novel missence mutation in FGFR3 gene in an Iranian family with LADD syndrome by Next-Generation Sequencing.

Amir Hooshang Bavarsad, Saeed Tizno, Farideh Ghanbari Mardasi, Javad Mohammadi Asl, Farah Talebi

International journal of pediatric otorhinolaryngology 2017;97():192-196

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Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing.

Nan Hong, Yan-hua Chen, Chen Xie, Bai-sheng Xu, Hui Huang, Xin Li, Yue-qing Yang, Ying-ping Huang, Jian-lian Deng, Ming Qi, Yang-shun Gu

Journal of Zhejiang University. Science. B 2015;15(8):727-34

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Results: 1 – 9 / 9

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Results for ""Tooth Abnormalities""[mesh_terms]

Third case of cerebral, ocular, dental, auricular, skeletal anomalies (CODAS) syndrome, further delineating a new malformation syndrome: first report of an affected male and review of literature.

Smith-Lemli-Opitz syndrome: a review, case report and dental implications.

Oral and craniofacial findings in a patient with methylmalonic aciduria and homocystinuria: review and a case report.

Two novel GJA1 variants in oculodentodigital dysplasia.

Novel ocular findings in oculodentodigital dysplasia (ODDD): a case report and literature review.

Rare Germline Variants in the Adenomatous Polyposis Coli Gene Associated with Dental and Osseous Anomalies.

Ion channels, channelopathies, and tooth formation.

Identification of a novel missence mutation in FGFR3 gene in an Iranian family with LADD syndrome by Next-Generation Sequencing.

Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing.

Results for
""Tooth Abnormalities""[mesh_terms]