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Identification of a hot spot for microgdeletions in patients with X-linked deafness type 3 (DFN3) 900kb proximal to the DFN3 gene POU3F4.

deKok, YJM (author)
Vossenaar, E (author)
Cremers, C (author)
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Dahl, N (author)
Uppsala universitet,Institutionen för genetik och patologi
Laporte, J (author)
Hu, L (author)
Lacombe, D (author)
Fischel-Ghodsian, (author)
Friedman, R (author)
Parnes, L (author)
Thorpe, P (author)
Malcolm, S (author)
Pander, HJ (author)
Heilbronner, H (author)
Gravelin, J (author)
den Dunnen, J (author)
Brunner, HG (author)
Ropers, HH (author)
Cremers, FPM (author)
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 (creator_code:org_t)
1996
1996
English.
In: Hum Mol Genet. ; 5, s. 1229-
  • Journal article (peer-reviewed)
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