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Literature DB >> 9529357

A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.

W Ahmad, V Brancolini, M F ul Faiyaz, H Lam, S ul Haque, M Haider, A Maimon, V M Aita, J Owen, D Brown, D J Zegarelli, M Ahmad, J Ott, A M Christiano.

Abstract

Entities: Disease Gene

Mesh：

Year: 1998 PMID： 9529357 PMCID： PMC1377039 DOI： 10.1086/301799

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

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18 in total

1. De novo inv(2)(p12q34) associated with Klippel-Feil anomaly and hypodontia.

Authors: Manolis J Papagrigorakis; Philippos N Synodinos; Constandinos P Daliouris; Caterina Metaxotou
Journal: Eur J Pediatr Date: 2003-06-24 Impact factor: 3.183

Review 2. Developmental disorders of the dentition: an update.

Authors: Ophir D Klein; Snehlata Oberoi; Ann Huysseune; Maria Hovorakova; Miroslav Peterka; Renata Peterkova
Journal: Am J Med Genet C Semin Med Genet Date: 2013-10-04 Impact factor: 3.908

Review 3. Monogenic Disorders of Adrenal Steroidogenesis.

Authors: Elizabeth S Baranowski; Wiebke Arlt; Jan Idkowiak
Journal: Horm Res Paediatr Date: 2018-06-06 Impact factor: 2.852

4. A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families.

Authors: Muhammad S Chishti; Dost Muhammad; Mahmud Haider; Wasim Ahmad
Journal: J Hum Genet Date: 2006-08-24 Impact factor: 3.172

10. Hypodontia prevalence and distribution pattern in a group of Qatari orthodontic and pediatric patients: A retrospective study.

Authors: Feras H Abed Al Jawad; Hanan Al Yafei; Muneera Al Sheeb; Buthaina Al Emadi; Najah Al Hashimi
Journal: Eur J Dent Date: 2015 Apr-Jun

A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.

1. De novo inv(2)(p12q34) associated with Klippel-Feil anomaly and hypodontia.

Review 2. Developmental disorders of the dentition: an update.

Review 3. Monogenic Disorders of Adrenal Steroidogenesis.

4. A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families.

Review 5. Genetic background of nonsyndromic oligodontia: a systematic review and meta-analysis.

6. Numerical abnormalities of permanent dentition - a case report.

7. Oligodontia is caused by mutation in LTBP3, the gene encoding latent TGF-beta binding protein 3.

8. A Nonsyndromic Autosomal Dominant Oligodontia with A Novel Mutation of PAX9-A Clinical and Genetic Report.

9. Asyndromic hypodontia associated with tooth morphology alteration: A rare case report.

10. Hypodontia prevalence and distribution pattern in a group of Qatari orthodontic and pediatric patients: A retrospective study.