Literature DB >> 28764250

Microtia in All the Siblings of a Family: A Rare Case.

Somashekar Gejje1, Brijesh Mishra2, Amrita Anandkumar Hongal3.   

Abstract

Entities:  

Keywords:  Congenital; Deformity; Ear; Genetics

Year:  2017        PMID： 28764250      PMCID： PMC5535441          DOI： 10.7860/JCDR/2017/24346.10035

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


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  3 in total

1.  Trisomies 13 and 18: prenatal diagnosis and epidemiologic studies in Hawaii, 1986-1997.

Authors:  M B Forrester; R D Merz
Journal:  Genet Test       Date:  1999

2.  In utero exposure to mycophenolate mofetil: a characteristic phenotype?

Authors:  Antonio Perez-Aytes; Ana Ledo; Virginia Boso; Pilar Sáenz; Eva Roma; José Luis Poveda; Maximo Vento
Journal:  Am J Med Genet A       Date:  2008-01-01       Impact factor: 2.802

3.  Microtia in Finland: comparison of characteristics in different populations.

Authors:  Samuli Suutarla; Jorma Rautio; Annukka Ritvanen; Sirpa Ala-Mello; Jussi Jero; Tuomas Klockars
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2007-06-04       Impact factor: 1.675
  3 in total
  1 in total

1.  Whole-Exome Sequencing of Discordant Monozygotic Twin Families for Identification of Candidate Genes for Microtia-Atresia.

Authors:  Xinmiao Fan; Lu Ping; Hao Sun; Yushan Chen; Pu Wang; Tao Liu; Rui Jiang; Xuegong Zhang; Xiaowei Chen
Journal:  Front Genet       Date:  2020-10-22       Impact factor: 4.599
  1 in total

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