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English |
ÖÐÎÄ |
English |
ÖÐÎÄ |
albinism |
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heredity |
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cancer family |
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heritability |
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cancer genetics |
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human biochemical genetics |
ÈËÀàÉú»¯ÒÅ´«Ñ§ |
carrier |
Я´øÕߣ¬ÔØÁ÷×Ó£¬ÔØÌ壬´ø³æÕß |
human cytogenetics |
ÈËÀàϸ°ûÒÅ´«Ñ§ |
cat cry syndrome |
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human molecular genetics |
ÈËÀà·Ö×ÓÒÅ´«Ñ§ |
deletion |
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human population genetics |
ÈËÀàȺÌåÒÅ´«Ñ§ |
diandry |
Ë«ÐÛÊܾ« |
inborn errors of metabolism |
ÏÈÌìÐÔ´úлȱÏÝ |
digyny |
Ë«´ÆÊܾ« |
invertion |
µ¹Î» |
Edwards's syndrome |
18ÈýÌå×ÛºÏÕ÷ |
isochromosome |
µÈ±ÛȾɫÌå |
endoreduplication |
ºËÄÚ¸´ÖÆ |
marker chromosome |
±ê¼ÇȾɫÌå |
eugenics |
ÓÅÉúѧ |
medical genetics |
ҽѧÒÅ´«Ñ§ |
familial carcinoma |
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medical genetics |
ҽѧÒÅ´«Ñ§ |
fragile site |
´àÐÔ²¿Î» |
modal number |
ÖÚÊý |
fragile X syndrome |
´àÐÔXȾɫÌå×ÛºÏÕ÷ |
molecular disease |
·Ö×Ó²¡ |
fusion gene |
ÈںϻùÒò |
monogenic disease |
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gene cluster |
»ùÒò´Ø |
mosaic |
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gene diagnosis |
»ùÒòÕï¶Ï |
multiple alleles |
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gene frequency |
»ùÒòƵÂÊ |
negative eugenics |
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gene maping, gene assignment |
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nucleosome |
ºËСÌå |
gene pool |
»ùÒò¿â |
oncogene |
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gene therapy |
»ùÒòÖÎÁÆ |
pedigree |
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genetic epidemiology |
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polygenic disease |
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genetic load |
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polygenic inheritance |
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genic disease |
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positive eugenics |
ÕýÓÅÉúѧ |
genotype frequency |
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satellite |
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hemoglobinopathy |
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somatic cell genetics |
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hereditary disease, inherited disease, genetic disease |
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structural aberration |
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hereditary enzympathy |
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thalassemia |
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