Literature DB >> 27891493

Mohr-Claussen Syndrome: A Rare Case.

Manjiri Uttam Joshi1, Namish Jagdish Chandra Batra2, Ankita Pradeep Patel3.   

Abstract

Entities:  

Keywords:  Developmental defects; Facial; Oral

Year:  2016        PMID: 27891493      PMCID: PMC5121831          DOI: 10.7860/JCDR/2016/22381.8635

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


× No keyword cloud information.
  6 in total

1.  [Hereditary abnormality of the buccal mucosa: abnormal bands and frenula].

Authors:  J PSAUME
Journal:  Revue Stomatol       Date:  1954-04

2.  Oro-facial-digital syndrome type II.

Authors:  Meenakshi Kalyan; S Kanitkar; Robby John; G Gireesh; Amit Bhate; M Mithun
Journal:  J Assoc Physicians India       Date:  2012-10

3.  Oral-facial-digital syndrome type II (Mohr syndrome): clinical and genetic manifestations.

Authors:  Naohiko Sakai; Nobuaki Nakakita; Yasuharu Yamazaki; Kenji Ui; Eiju Uchinuma
Journal:  J Craniofac Surg       Date:  2002-03       Impact factor: 1.046

4.  The oro-facial-digital syndrome--manifestations in the oral cavity--case report.

Authors:  Y T Silva Sousa; D D Kanaan
Journal:  Braz Dent J       Date:  1994

5.  Mohr-Claussen syndrome or oro-facial-digital syndrome (OFDS) type-II.

Authors:  Arnab Biswas; Jayanta K Ghosh; Malay K R Sinha; Kaberi Basu; Sukanta Chatterjee
Journal:  J Pak Med Assoc       Date:  2009-07       Impact factor: 0.781

6.  Orofaciodigital syndrome, type I: a phenotypic and genetic analysis.

Authors:  M Melnick; E D Shields
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1975-11
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.