(Q50507468)

English

Usher syndrome in the Samaritans: strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders.

scientific article published in October 1997

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

Usher syndrome in the Samaritans: strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

1 reference

based on heuristic

inferred from title

author name string

Bonné-Tamir B

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

Nystuen A

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

Seroussi E

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

Kalinsky H

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

Kwitek-Black AE

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

Korostishevsky M

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

Adato A

7

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

Sheffield VC

8

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

publication date

1 October 1997

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

American Journal of Biological Anthropology

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

104

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

193-200

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

RPS2 of Arabidopsis thaliana: a leucine-rich repeat class of plant disease resistance genes

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Genes and phenotypes in the Samaritan isolate

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Are there Hebrews left?

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Digital dermatoglyphics of the Samaritans

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Genetic mapping of the gene for Usher syndrome: linkage analysis in a large Samaritan kindred.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Localization of Usher syndrome type II to chromosome 1q.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

The A. thaliana disease resistance gene RPS2 encodes a protein containing a nucleotide-binding site and leucine-rich repeats

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Localization of two genes for Usher syndrome type I to chromosome 11.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

The product of the tobacco mosaic virus resistance gene N: similarity to toll and the interleukin-1 receptor

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Genetic evolution of the Samaritans

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

New gene in the homologous human 11q13-q14 and mouse 7F chromosomal regions

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Reproduction and inbreeding among the Samaritans

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8644%28199710%29104%3A2%3C193%3A%3AAID-AJPA5%3E3.0.CO%3B2-%23

21 January 2018

Identifiers

10.1002/(SICI)1096-8644(199710)104:2<193::AID-AJPA5>3.0.CO;2-#

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/9386826

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