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Literature DB >> 2248525

The genetics of deafness.

W Reardon¹, M Pembrey.

Abstract

Entities: Disease

Mesh：

Year: 1990 PMID： 2248525 PMCID： PMC1792620 DOI： 10.1136/adc.65.11.1196

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

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12 in total

1. The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK.

Authors: H G Brunner; A van Bennekom; E M Lambermon; T L Oei; W R Cremers; B Wieringa; H H Ropers
Journal: Hum Genet Date: 1988-12 Impact factor: 4.132

2. Identification of the cystic fibrosis gene: genetic analysis.

Authors: B Kerem; J M Rommens; J A Buchanan; D Markiewicz; T K Cox; A Chakravarti; M Buchwald; L C Tsui
Journal: Science Date: 1989-09-08 Impact factor: 47.728

3. Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen gene.

Authors: R G Knowlton; E J Weaver; A F Struyk; W H Knobloch; R A King; K Norris; A Shamban; J Uitto; S A Jimenez; D J Prockop
Journal: Am J Hum Genet Date: 1989-11 Impact factor: 11.025

4. X-linked mixed deafness with stapes fixation in a Mauritian kindred: linkage to Xq probe pDP34.

Authors: C Wallis; R Ballo; G Wallis; P Beighton; J Goldblatt
Journal: Genomics Date: 1988-11 Impact factor: 5.736

5. The Stickler syndrome: evidence for close linkage to the structural gene for type II collagen.

Authors: C A Francomano; R M Liberfarb; T Hirose; I H Maumenee; E A Streeten; D A Meyers; R E Pyeritz
Journal: Genomics Date: 1987-12 Impact factor: 5.736

6. Marshall/Stickler syndrome.

Authors: M Baraitser
Journal: J Med Genet Date: 1982-04 Impact factor: 6.318

7. Childhood deafness in the European community.

Authors: J A Martin; O Bentzen; J R Colley; D Hennebert; C Holm; S Iurato; G A de Jonge; O McCullen; M L Meyer; W J Moore; A Morgon
Journal: Scand Audiol Date: 1981

8. Genetic heterogeneity in osteogenesis imperfecta.

Authors: D O Sillence; A Senn; D M Danks
Journal: J Med Genet Date: 1979-04 Impact factor: 6.318

9. Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.

Authors: C Foy; V Newton; D Wellesley; R Harris; A P Read
Journal: Am J Hum Genet Date: 1990-06 Impact factor: 11.025

10. Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2.

Authors: B Sykes; D Ogilvie; P Wordsworth; G Wallis; C Mathew; P Beighton; A Nicholls; F M Pope; E Thompson; P Tsipouras
Journal: Am J Hum Genet Date: 1990-02 Impact factor: 11.025

3 in total

1. Inherited deafness in childhood--the genetic revolution unmasks the clinical challenge.

Authors: W Reardon; R F Mueller
Journal: Arch Dis Child Date: 2000-04 Impact factor: 3.791

Review 2. Genetic deafness.

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

3. Hearing screening in children--state of the art(s)

Authors: R R Phillips; P D Phelps
Journal: Arch Dis Child Date: 1991-04 Impact factor: 3.791

3 in total