About: Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population     Goto   Sponge   NotDistinct   Permalink

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  • Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population
  • Dvojitá heterozygosita s mutacemi postihujícími oba GJB2 a GJB6 geny je možnou, ale velmi vzácnou příčinou vrozené hluchoty v české populaci (cs)
  • Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population (en)
Title
  • Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population
  • Dvojitá heterozygosita s mutacemi postihujícími oba GJB2 a GJB6 geny je možnou, ale velmi vzácnou příčinou vrozené hluchoty v české populaci (cs)
  • Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population (en)
skos:prefLabel
  • Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population
  • Dvojitá heterozygosita s mutacemi postihujícími oba GJB2 a GJB6 geny je možnou, ale velmi vzácnou příčinou vrozené hluchoty v české populaci (cs)
  • Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population (en)
skos:notation
  • RIV/00216208:11130/05:00004102!RIV06-MSM-11130___
http://linked.open.../vavai/riv/strany
  • 9;14
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(NM7417), Z(MSM 111300003)
http://linked.open...iv/cisloPeriodika
  • 1
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 518704
http://linked.open...ai/riv/idVysledku
  • RIV/00216208:11130/05:00004102
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • Double; Heterozygosity; Mutations; Involving; Genes; Possible; Cause; Congenital; Deafness; Czech; Population (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [C5424418ABD3]
http://linked.open...i/riv/nazevZdroje
  • Annals of Human Genetics
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 69
http://linked.open...iv/tvurceVysledku
  • Kabelka, Zdeněk
  • Seeman, Pavel
  • Groh, Daniel
http://linked.open...n/vavai/riv/zamer
issn
  • 0003-4800
number of pages
http://localhost/t...ganizacniJednotka
  • 11130
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