BanI/D13S141/D13S175 represents a novel informative haplotype at the GJB2 gene region in the Iranian population.

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BanI/D13S141/D13S175 represents a novel informative haplotype at the GJB2 gene region in the Iranian population.

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http://www.wikidata.org/entity/Q50434397

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2011 nî lūn-bûn

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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BanI/D13S141/D13S175 represent ...... ion in the Iranian population.

@en

BanI/D13S141/D13S175 represent ...... ion in the Iranian population.

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type

Item

label

BanI/D13S141/D13S175 represent ...... ion in the Iranian population.

@en

BanI/D13S141/D13S175 represent ...... ion in the Iranian population.

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prefLabel

BanI/D13S141/D13S175 represent ...... ion in the Iranian population.

@en

BanI/D13S141/D13S175 represent ...... ion in the Iranian population.

@nl

P1476

BanI/D13S141/D13S175 represent ...... ion in the Iranian population.

@en

P2093

Halimeh Rezaei

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Sadeq Vallian

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P2860

Haplotype of multiple polymorphisms resolved by enzymatic amplification of single DNA molecules.

A comparison of phasing algorithms for trios and unrelated individuals.

Haplotype analysis in population genetics and association studies.

The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population.

Molecular haplotyping of genetic markers 10 kb apart by allele-specific long-range PCR.

Absence of mutations in GJB2 (Connexin-26) gene in an ethnic group of southwest Iran.

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.

Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East.

Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians.

A new large deletion in the DFNB1 locus causes nonsyndromic hearing loss.

P2888

s10571-011-9683-4

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749-754

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scholarly article

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10.1007/S10571-011-9683-4

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P433

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P478

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P577

2011-04-12T00:00:00Z

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P698

21484343

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