Literature DB >> 7286990

Autosomal recessive "uncomplicated" profound childhood deafness in an Arabic family with high consanguinity.

A Kabarity, S A Al-Awadi, T I Farag, G Mallalah.   

Abstract

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Year:  1981        PMID： 7286990     DOI： 10.1007/BF00281704

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  5 in total

Review 1.  PROFOUND CHILDHOOD DEAFNESS.

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

2.  A note on deaf mutism.

Authors:  C S CHUNG; O W ROBINSON; N E MORTON
Journal:  Ann Hum Genet       Date:  1959-12       Impact factor: 1.670

3.  Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death.

Authors:  A JERVELL; F LANGE-NIELSEN
Journal:  Am Heart J       Date:  1957-07       Impact factor: 4.749

4.  A genetic register system (RAPID).

Authors:  A E Emery; D Elliott; M Moores; C Smith
Journal:  J Med Genet       Date:  1974-06       Impact factor: 6.318

5.  Two types of congenital recessive deafness.

Authors:  M C Mengel; B W Konigsmark; V A McKusick
Journal:  Eye Ear Nose Throat Mon       Date:  1969-05
  5 in total
  2 in total

Review 1.  Autosomal recessive disorders among Arabs: an overview from Kuwait.

Authors:  A S Teebi
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

Review 2.  Hereditary disorders in the Eastern Mediterranean Region.

Authors:  H Hamamy; A Alwan
Journal:  Bull World Health Organ       Date:  1994       Impact factor: 9.408
  2 in total

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