Literature DB >> 5006530

A high risk registry to find congenital deafness.

L Bergstrom, W G Hemenway, M P Downs.   

Abstract

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Year:  1971        PMID： 5006530

Source DB:  PubMed          Journal:  Otolaryngol Clin North Am        ISSN： 0030-6665            Impact factor:   3.346


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  10 in total

1.  DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24.

Authors:  C C Greene; P M McMillan; S E Barker; P Kurnool; M I Lomax; M Burmeister; M M Lesperance
Journal:  Am J Hum Genet       Date:  2000-12-11       Impact factor: 11.025

Review 2.  Genetic deafness.

Authors:  W Reardon
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

3.  Variations in genetic assessment and recurrence risks quoted for childhood deafness: a survey of clinical geneticists.

Authors:  M J Parker; H Fortnum; I D Young; A C Davis
Journal:  J Med Genet       Date:  1999-02       Impact factor: 6.318

4.  Developmental hearing loss disrupts synaptic inhibition: implications for auditory processing.

Authors:  Anne E Takesian; Vibhakar C Kotak; Dan H Sanes
Journal:  Future Neurol       Date:  2009-05-01

5.  Refinement of the locus for non-syndromic sensorineural deafness (DFN2).

Authors:  Bin Cui; Haibing Zhang; Yongzhong Lu; Wei Zhong; Gang Pei; Xiangyin Kong; Landian Hu
Journal:  J Genet       Date:  2004-04       Impact factor: 1.166

6.  A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies.

Authors:  Daniel R Jensen; Donna M Martin; Stephen Gebarski; Trilochan Sahoo; Ellen K Brundage; A Craig Chinault; Edgar A Otto; Moumita Chaki; Friedhelm Hildebrandt; Sau Wai Cheung; Marci M Lesperance
Journal:  Am J Med Genet A       Date:  2009-03       Impact factor: 2.802

Review 7.  Identification of impaired hearing in early childhood.

Authors:  D Wong; C P Shah
Journal:  Can Med Assoc J       Date:  1979-09-08       Impact factor: 8.262

8.  Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.

Authors:  Zubair M Ahmed; Saima Riazuddin; Sandar Aye; Rana A Ali; Hanka Venselaar; Saima Anwar; Polina P Belyantseva; Muhammad Qasim; Sheikh Riazuddin; Thomas B Friedman
Journal:  Hum Genet       Date:  2008-08-22       Impact factor: 4.132

9.  A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from Pakistan.

Authors:  Muhammad Ansar; Mohammad Amin ud Din; Muhammad Arshad; Muhammad Sohail; Mohammad Faiyaz-Ul-Haque; Sayedul Haque; Wasim Ahmad; Suzanne M Leal
Journal:  Eur J Hum Genet       Date:  2003-01       Impact factor: 4.246

10.  Consanguinity Among Parents of Iranian Deaf Children.

Authors:  Mohammad Ajallouyan; Shokofeh Radfar; Sima Nouhi; Seid Abbas Tavallaie; Susan Amirsalari; Jaleh Yousefi; Mahdieh Hasanali Fard
Journal:  Iran Red Crescent Med J       Date:  2016-08-07       Impact factor: 0.611
  10 in total

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