Literature DB >> 13917431

A deafmute with two congenital syndromes.

F M STOLLER.   

Abstract

Keywords:  DEAF-MUTISM/complications; EYE/abnormalities; SCAPULA/abnormalities

Mesh：

Year:  1962        PMID： 13917431     DOI： 10.1001/archotol.1962.00740050046008

Source DB:  PubMed          Journal:  Arch Otolaryngol        ISSN： 0003-9977


× No keyword cloud information.
  4 in total

Review 1.  PROFOUND CHILDHOOD DEAFNESS.

Authors:  G R FRASER
Journal:  J Med Genet       Date:  1964-12       Impact factor: 6.318

Review 2.  Heterogeneity in Waardenburg syndrome.

Authors:  M J Hageman; J W Delleman
Journal:  Am J Hum Genet       Date:  1977-09       Impact factor: 11.025

3.  Waardenburg's memorial lecture: Waardenburg's syndrome.

Authors:  J François
Journal:  Int Ophthalmol       Date:  1982-05       Impact factor: 2.031

4.  Degeneration of saccular hair cells caused by MITF gene mutation.

Authors:  Yi Du; Li-Li Ren; Qing-Qing Jiang; Xing-Jian Liu; Fei Ji; Yue Zhang; Shuo-Long Yuan; Zi-Ming Wu; Wei-Wei Guo; Shi-Ming Yang
Journal:  Neural Dev       Date:  2019-01-11       Impact factor: 3.842
  4 in total

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