Genotypic and phenotypic variation in six patients with solitary median maxillary central incisor syndrome-Reference-Cited by-同舟云学术

Genotypic and phenotypic variation in six patients with solitary median maxillary central incisor syndrome

Published:2015-06-16 Issue:10 Volume:167 Page:2451-2458
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Poelmans Simon¹,Kawamoto Tatsuro²³,Cristofoli Francesca⁴,Politis Constantinus⁵,Vermeesch Joris⁴,Bailleul-Forestier Isabelle⁶⁷,Hens Greet⁸,Devriendt Koenraad⁴,Verdonck Anna¹,Carels Carine¹²

Affiliation:

1. Department of Oral Health Sciences-Orthodontics; KU Leuven and Dentistry; University Hospitals Leuven; Leuven Belgium

2. Department of Orthodontics and Craniofacial Biology; College of Dentistry; Radboudumc Nijmegen The Netherlands

3. Department of Maxillofacial Reconstruction and Function; Maxillofacial Orthognathics; Division of Maxillofacial/Neck Reconstruction; Graduate School; Tokyo Medical and Dental University; Tokyo Japan

4. Department of Human Genetics; KU Leuven and Centre for Human Genetics; University Hospitals Leuven; Leuven Belgium

5. Department of Oral and Maxillofacial Surgery; KU Leuven and University Hospitals Leuven; Leuven Belgium

6. Department of Oral Health Sciences-Paediatric Dentistry and Special Care; KU Leuven and Dentistry; University Hospitals Leuven; Leuven Belgium

7. Department of Paediatric Dentistry; Paul Sabatier University; Hôpitaux de Toulouse France

8. Department of Otorhinolaryngology; Head and Neck Surgery; KU Leuven and University Hospitals Leuven; Leuven Belgium

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37207/fullpdf

Reference36 articles.

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3. Familial ring (18) mosaicism in a 23-year-old young adult with 46,XY,r(18) (::p11->q21::)/46,XY karyotype, intellectual disability, motor retardation and single maxillary incisor and in his phenotypically normal mother, karyotype 47,XX,+r(18)(::p11-;Balci;Am J Med Genet A,2011

4. Solitary upper incisor, hypopituitarism and monosomy 18p chromosome aberration;Boudailliez;J Genet Hum,1983

5. Prenatal diagnosis of partial trisomy 3p(3p23->pter) and monosomy 7q(7q36-;Chen;Prenat Diagn,1999

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