Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel.

Literature DB >> 7573061

Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel.

D A Scott, R Carmi, K Elbedour, G M Duyk, E M Stone, V C Sheffield.

Abstract

Entities: Disease Gene

Mesh：

Substances：

Year: 1995 PMID： 7573061 PMCID： PMC1801487

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

× No keyword cloud information.

12 in total

1. The gene for an inherited form of deafness maps to chromosome 5q31.

Authors: P E Leon; H Raventos; E Lynch; J Morrow; M C King
Journal: Proc Natl Acad Sci U S A Date: 1992-06-01 Impact factor: 11.205

2. A family with X-linked deafness showing linkage to the proximal Xq region of the X chromosome.

Authors: D Robinson; M Lamont; G Curtis; D C Shields; P Phelps
Journal: Hum Genet Date: 1992-11 Impact factor: 4.132

3. Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness.

Authors: W Reardon; S Roberts; P D Phelps; N S Thomas; L Beck; R Issac; H E Hughes
Journal: Am J Med Genet Date: 1992-11-01

4. A microsatellite genetic linkage map of human chromosome 13.

Authors: K E Petrukhin; M C Speer; E Cayanis; M F Bonaldo; U Tantravahi; M B Soares; S G Fischer; D Warburton; T C Gilliam; J Ott
Journal: Genomics Date: 1993-01 Impact factor: 5.736

5. Integrated human genome-wide maps constructed using the CEPH reference panel.

Authors: K H Buetow; J L Weber; S Ludwigsen; T Scherpbier-Heddema; G M Duyk; V C Sheffield; Z Wang; J C Murray
Journal: Nat Genet Date: 1994-04 Impact factor: 38.330

Review 6. [Congenital sensorineural deafness and associated syndromes].

Authors: L Moatti; E N Garabedian; H Lacombe; C Spir-Jacob
Journal: Ann Otolaryngol Chir Cervicofac Date: 1990

7. Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families.

Authors: P Coucke; G Van Camp; B Djoyodiharjo; S D Smith; R R Frants; G W Padberg; J K Darby; E H Huizing; C W Cremers; W J Kimberling
Journal: N Engl J Med Date: 1994-08-18 Impact factor: 91.245

8. Linkage of a gene for dominant non-syndromic deafness to chromosome 19.

Authors: A H Chen; L Ni; K Fukushima; J Marietta; M O'Neill; P Coucke; P Willems; R J Smith
Journal: Hum Mol Genet Date: 1995-06 Impact factor: 6.150

9. A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.

Authors: P Guilford; H Ayadi; S Blanchard; H Chaib; D Le Paslier; J Weissenbach; M Drira; C Petit
Journal: Hum Mol Genet Date: 1994-06 Impact factor: 6.150

10. A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval.

Authors: H Chaïb; G Lina-Granade; P Guilford; H Plauchu; J Levilliers; A Morgon; C Petit
Journal: Hum Mol Genet Date: 1994-12 Impact factor: 6.150

14 in total

Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel.

1. The gene for an inherited form of deafness maps to chromosome 5q31.

2. A family with X-linked deafness showing linkage to the proximal Xq region of the X chromosome.

3. Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness.

4. A microsatellite genetic linkage map of human chromosome 13.

5. Integrated human genome-wide maps constructed using the CEPH reference panel.

Review 6. [Congenital sensorineural deafness and associated syndromes].

7. Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families.

8. Linkage of a gene for dominant non-syndromic deafness to chromosome 19.

9. A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.

10. A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval.

1. The Roots of Linguistic Organization in a New Language.

2. The emergence of grammar: systematic structure in a new language.

3. Deciphering the fine-structure of tribal admixture in the Bedouin population using genomic data.

Review 4. Gap junctions in inherited human disease.

Review 5. Nonsyndromic hearing impairment: unparalleled heterogeneity.

6. Persistence and transmission of recessive deafness and sign language: new insights from village sign languages.

7. Symbiotic symbolization by hand and mouth in sign language.

8. An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds.

Review 9. Relevance of connexin deafness (DFNB1) to human evolution.

10. Fitness among individuals with early childhood deafness: Studies in alumni families from Gallaudet University.