Linkage analysis has been carried out in a family with severe congenital sensorineural deafness with a structural abnormality of the inner ear. Recombinations show the gene responsible for deafness in this family to lie between the loci DXS255 (Xp11.22) and DXS94 (Xq22). Close linkage was found to locus DXS159 (cpX289) in Xq12, with a LOD score of 3.155 and 0 recombination. This location is consistent with other linkage studies of X-linked deafnes
PubMed ID: 9799605X-linked inherited hearing impairment is a group of heterogeneous disorders accoun...
Hearing impairment is an immensely diagnosed genetic cause, 5% of the total world population effects...
The identification of deafness genes is an essential step in understanding the molecular mechanism o...
Non-syndromic X-linked deafness is highly heterogeneous. At least five different clinical forms have...
Non-syndromic X-linked deafness is genetically heterogeneous but clinical and radiological studies h...
Sensorineural hearing loss is a very diffuse pathology (about 1/1000 born) with several types of tra...
Clinically significant hearing loss affects 1 in 1000 infants and it is estimated that at least 50 %...
To initiate a study on molecular characterization of non-syndromic recessive deafness in the Pakista...
The recessive mode of transmission accounts for ∼75 % of inherited non syndromic deafness cases. We ...
Hearing loss is a common sensory deficit in humans. The hearing loss may be conductive, sensorineura...
There are 68 sex-linked syndromes that include hearing loss as one feature and five sex-linked nonsy...
Hearing loss is one of the most frequent sensory disorders in humans. Haplotype reconstruction is on...
We have found that the microsatellite marker AFM207zg5 (DXS995) maps to all previously described del...
The X-linked deafness of Nance is present in a South African kindred. Recognition of the familial pa...
The pathophysiology of sensorineural hearing impairment, which is a common clinical disorder, remain...
PubMed ID: 9799605X-linked inherited hearing impairment is a group of heterogeneous disorders accoun...
Hearing impairment is an immensely diagnosed genetic cause, 5% of the total world population effects...
The identification of deafness genes is an essential step in understanding the molecular mechanism o...
Non-syndromic X-linked deafness is highly heterogeneous. At least five different clinical forms have...
Non-syndromic X-linked deafness is genetically heterogeneous but clinical and radiological studies h...
Sensorineural hearing loss is a very diffuse pathology (about 1/1000 born) with several types of tra...
Clinically significant hearing loss affects 1 in 1000 infants and it is estimated that at least 50 %...
To initiate a study on molecular characterization of non-syndromic recessive deafness in the Pakista...
The recessive mode of transmission accounts for ∼75 % of inherited non syndromic deafness cases. We ...
Hearing loss is a common sensory deficit in humans. The hearing loss may be conductive, sensorineura...
There are 68 sex-linked syndromes that include hearing loss as one feature and five sex-linked nonsy...
Hearing loss is one of the most frequent sensory disorders in humans. Haplotype reconstruction is on...
We have found that the microsatellite marker AFM207zg5 (DXS995) maps to all previously described del...
The X-linked deafness of Nance is present in a South African kindred. Recognition of the familial pa...
The pathophysiology of sensorineural hearing impairment, which is a common clinical disorder, remain...
PubMed ID: 9799605X-linked inherited hearing impairment is a group of heterogeneous disorders accoun...
Hearing impairment is an immensely diagnosed genetic cause, 5% of the total world population effects...
The identification of deafness genes is an essential step in understanding the molecular mechanism o...