File:X recessive carrier mother ku.svg

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Description Kurdishː Nexweşiya rengkoriya sor û kesk, nexweşiyek bomaweyî ye, ji aliyê allên bezîw ên li ser kromozoma X a herdu bavanan diguhaze weçeyan.Ji ber ko di nêran de ji kromozoma X-ê tenê yek heye, nexweşî herî zêde di kesên nêr de peyda dibe.Divê mê ji herdu bavanên xwe allela mutant a bezîw werbigre ko sîfetê di rûxsara xwe de xuya bike. Gava ji bavanek allela mutant a bezîw, ji bavanê din allela zal biguhaze bo weçeya mê, ji ber bandora allela zal, nexweşî peyda nabe.
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Source https://openstax.org/details/books/biology.
Author https://openstax.org

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Public domain I, the copyright holder of this work, release this work into the public domain. This applies worldwide.
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current07:24, 16 March 2023Thumbnail for version as of 07:24, 16 March 2023955 × 965 (85 KB)Biyolojiyabikurdi (talk | contribs){{Information |Description= Kurdishː Nexweşiya rengkoriya sor û kesk, nexweşiyek bomaweyî ye, ji aliyê allên bezîw ên li ser kromozoma X a herdu bavanan diguhaze weçeyan.Ji ber ko di nêran de ji kromozoma X-ê tenê yek heye, nexweşî herî zêde di kesên nêr de peyda dibe.Divê mê ji herdu bavanên xwe allela mutant a bezîw werbigre ko sîfetê di rûxsara xwe de xuya bike. Gava ji bavanek allela mutant a bezîw, ji bavanê din allela zal biguhaze bo weçeya mê, ji ber bandora allela zal, nexweşî peyda n...

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