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DEAFNESS, AUTOSOMAL RECESSIVE 15

Known as: DFNB72, DEAFNESS, AUTOSOMAL RECESSIVE 95, DFNB15 
 
National Institutes of Health

Papers overview

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2014
2014
With homozygosity mapping we have identified two large homozygous regions on chromosome 3q13.11–q13.31 and chromosome 19p13.3–q31… Expand
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2008
2008
BACKGROUND Non-syndromic hearing loss is the most genetically heterogeneous trait known in humans. To date, 54 loci for autosomal… Expand
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2007
2007
ZusammenfassungHintergrundDer nichtsyndromale Hörverlust ist die Erkrankung, für die beim Menschen bislang die häufigsten… Expand
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Review
2003
Review
2003
Congenital hearing loss has been documented to occur in 1 of 1000 live births, with over half of these cases predicted to be… Expand
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2001
2001
BACKGROUND Earlier studies have mapped the autosomal recessive nonsyndromic deafness locus, DFNB15, to chromosomes 3q21.3-q25.2… Expand
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2001
2001
Background: Earlier studies have mapped the autosomal recessive nonsyndromic deafness locus, DFNB15, to chromosomes 3q21.3-q25.2… Expand
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