Hormones and Heredity by J. T. Cunningham
page 110 of 228 (48%)
page 110 of 228 (48%)
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White-eyed male Red-eyed female XW XW x XR YW F1 Red-eyed male White-eyed female XW XR XW YW F2 White-eyed male Red-eyed male White-eyed female Red-eyed female XW XW XR XW XW YW XR YW Homozygous. Heterozygous. Homozygous. Heterozygous. It must be explained that according to this theory the normal male is always heterozygous, because the _Y_ chromosome never carries any other factor except that for sex; it is thus of no more importance than the absence of an _X_ chromosome which occurs in those cases where the male has one sex-chromosome and the female two. According to the researches of von Winiwarter [Footnote: 'Spermatogenese humaine,' _Arch. de Biol._, xxvii., 1912.] on spermatogenesis in man, the latter is actually the case in the human species. This investigator found that there were 48 chromosomes in the female cell, 47 in the male; after the reduction divisions the unfertilised ova had 24 chromosomes, half the spermatids 24 and half 23, so that sex is determined in man by the spermatozoon. Morgan believes that the heredity of haemophilia (the constitutional defect which prevents the spontaneous cessation of bleeding) follows the same scheme, and also at least some forms of stationary night-blindness-- that is, the inability to see in twilight. We may mention a few other in animals, referring the reader for a fuller account to the works cited. One example in the barred character of the |
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