Scribd Logo
Upload

Welcome to Scribd!

  • Brochure Human Genetics

    Uploaded by

    Eldimson Bermudo
    2 views1 page
    A la fo ae s I es nctu n ge pi im cr his newly discovered genetic disorder obeys autosomal recessive inheritance pattern. The individual must have the 2 copies of mutant allele to express the syndrome. If the individual has only one, he will only be a carrier and hence, does not develop the condition. When two carriers mate, each child has a 25% chance of being homozygous wild-type (unaffected);

    Original Description:

    Copyright

    © Attribution Non-Commercial (BY-NC)

    Available Formats

    PDF, TXT or read online from Scribd

    Did you find this document useful?

    Is this content inappropriate?

    Report this Document
    A la fo ae s I es nctu n ge pi im cr his newly discovered genetic disorder obeys autosomal recessive inheritance pattern. The individual must have the 2 copies of mutant allele to express the syndrome. If the individual has only one, he will only be a carrier and hence, does not develop the condition. When two carriers mate, each child has a 25% chance of being homozygous wild-type (unaffected);

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as PDF, TXT or read online from Scribd
    Flag for inappropriate content
    2 views1 page

    Brochure Human Genetics

    Uploaded by

    Eldimson Bermudo
    A la fo ae s I es nctu n ge pi im cr his newly discovered genetic disorder obeys autosomal recessive inheritance pattern. The individual must have the 2 copies of mutant allele to express the syndrome. If the individual has only one, he will only be a carrier and hence, does not develop the condition. When two carriers mate, each child has a 25% chance of being homozygous wild-type (unaffected);

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as PDF, TXT or read online from Scribd
    Flag for inappropriate content
    of 1

    A

    la fo ae s i es nctu n ge pi

    im cr

    ET E M M O O S R R M D D O Y Y T S S P Y M Y Y M M S A A M M A A H H
    al

    w pr i d o s t e a n hou rud - s pr d lde ing e t od t rs uc h e , fr ears e e t i ag , s y ea n a ile lo e s rs b i bo pin , lit n g y es to .

    e, es on d r b an l tu ea art, lls, i a f g e ial he e c f a c d i n e c v fa he ti o l u rs al in t duc n i i n c spa e r e m a v r o , no cts epr c r s , nce s e b a fe , r y i s m ne s , de ood l a p h omi r o w bl i s p o r pr e b d y s m ce e y . d idfa a l hus m t e r ant l a lec te

    his newly discovered genetic disorder obeys autosomal recessive inheritance pattern. Thus, the individual must have the 2 copies of mutant allele to express the syndrome. If the individual has only one, he will only be a carrier and hence, does not develop the condition. (unaffected carrier). When two carriers mate, each child has a 25% chance of being homozygous wild-type (unaffected); a 25% chance of being homozygous mutant (affected); or a 50% chance of being heterozygous (unaffected carrier).

    You might also like