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                                                      »ù´¡Ò½Ñ§´Ê»ã | 
                         
                       
                    
                    
                            	
                    
                            	
                    
                    
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                              ҽѧÒÅ´«Ñ§´Ê»ã | 
             
           
          
          
            
              
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 English  | 
 ÖÐÎÄ  | 
 English  | 
 ÖÐÎÄ  |  
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 albinism  | 
 °×»¯²¡  | 
 heredity  | 
 ÒÅ´«  |  
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 cancer family  | 
 °©¼Ò×å  | 
 heritability  | 
 ÒÅ´«ÂÊ  |  
| 
 cancer genetics  | 
 Ö×ÁöÒÅ´«Ñ§  | 
 human biochemical genetics  | 
 ÈËÀàÉú»¯ÒÅ´«Ñ§  |  
| 
 carrier  | 
 Я´øÕߣ¬ÔØÁ÷×Ó£¬ÔØÌ壬´ø³æÕß  | 
 human cytogenetics  | 
 ÈËÀàϸ°ûÒÅ´«Ñ§  |  
| 
 cat cry syndrome  | 
 è½Ð×ÛºÏÕ÷  | 
 human molecular genetics  | 
 ÈËÀà·Ö×ÓÒÅ´«Ñ§  |  
| 
 deletion  | 
 ȱʧ  | 
 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  | 
 ¼Ò×åÐÔ°©  | 
 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  | 
 µ¥»ùÒò²¡  |  
| 
 gene cluster  | 
 »ùÒò´Ø  | 
 mosaic  | 
 ǶºÏÌå  |  
| 
 gene diagnosis  | 
 »ùÒòÕï¶Ï  | 
 multiple alleles  | 
 ¸´µÈλ»ùÒò  |  
| 
 gene frequency  | 
 »ùÒòƵÂÊ  | 
 negative eugenics  | 
 ¸ºÓÅÉúѧ  |  
| 
 gene maping, gene assignment  | 
 »ùÒò¶¨Î»  | 
 nucleosome  | 
 ºËСÌå  |  
| 
 gene pool  | 
 »ùÒò¿â  | 
 oncogene  | 
 °©»ùÒò£¬Ô°©»ùÒò  |  
| 
 gene therapy  | 
 »ùÒòÖÎÁÆ  | 
 pedigree  | 
 ϵÆ×  |  
| 
 genetic epidemiology  | 
 ÒÅ´«²¡Á÷ÐÐѧ  | 
 polygenic disease  | 
 ¶à»ùÒò²¡  |  
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 genetic load  | 
 ÒÅ´«¸ººÉ  | 
 polygenic inheritance  | 
 ¶à»ùÒòÒÅ´«  |  
| 
 genic disease  | 
 »ùÒò²¡  | 
 positive eugenics  | 
 ÕýÓÅÉúѧ  |  
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 genotype frequency  | 
 »ùÒòÐÍÆµÂÊ  | 
 satellite  | 
 ÎÀÐÇ£¬ËæÌå  |  
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 hemoglobinopathy  | 
 Ѫºìµ°°×²¡  | 
 somatic cell genetics  | 
 Ìåϸ°ûÒÅ´«Ñ§  |  
| 
 hereditary disease, inherited disease, genetic disease  | 
 ÒÅ´«²¡  | 
 structural aberration  | 
 ½á¹¹»û±ä  |  
| 
 hereditary enzympathy  | 
 ÒÅ´«ÐÔø²¡  | 
 thalassemia  | 
 º£ÑóÐÔÆ¶Ñª  |    | 
             
           
		  
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