Literature DB >> 3321996

The Nager syndrome.

J T Hecht1, L L Immken, L F Harris, S Malini, C I Scott.   

Abstract

The Nager syndrome was identified in a newborn infant and in a subsequent sib by prenatal ultrasonography. This report documents an autosomal recessive pattern of inheritance for this disorder.

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Year:  1987        PMID: 3321996     DOI: 10.1002/ajmg.1320270426

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

Review 1.  Nager acrofacial dysostosis.

Authors:  M T McDonald; J L Gorski
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

2.  Molecular mechanisms of hearing loss in Nager syndrome.

Authors:  Santosh Kumar Maharana; Jean-Pierre Saint-Jeannet
Journal:  Dev Biol       Date:  2021-04-14       Impact factor: 3.148

3.  A case report: nager acrofacial dysostosis.

Authors:  Shahin Abdollahi Fakhim; Nikzad Shahidi; Mehrnoush Mousaviagdas
Journal:  Iran J Otorhinolaryngol       Date:  2012
  3 in total

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