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A ÏÙÜÕÍѰ±Ã¸È±·¦Ö¢ adenosine deaminase deficiency (ADA) ÏÙ²¡¶¾ adenovirus Alagille×ÛºÏÕ÷ Alagille syndrome µÈλ»ùÒò allele °±»ùËá amino acids ¶¯ÎïÄ£ÐÍ animal model ¿¹Ìå antibody µòÍö apoptosis ·-°Í×ÛºÏÕ÷ ataxia-telangiectasia ³£È¾É«ÌåÏÔÐÔ autosomal dominant ³£È¾É«Ìå autosome B ϸ¾úÈ˹¤È¾É«Ìå bacterial artificial chromosome (BAC) ¼î»ù¶Ô base pair ÏÈÌìȱÏÝ birth defect ¹ÇËèÒÆÖ² bone marrow transplantation BRCA1/BRCA2 C °© cancer ºóÑ¡»ùÒò candidate gene °© carcinoma cDNAÎÄ¿â cDNA library ϸ°û cell ȾɫÌå chromosome ¿Ë¡ cloning ÃÜÂë codon ÌìÉúµÄ congenital ÖØµþȺ contig ÄÒÐÔÏËά»¯ cystic fibrosis ϸ°ûÒÅ´«Í¼ cytogenetic map D ȱʧ deletion ÍÑÑõºËÌǺËËá deoxyribonucleic acid (DNA) ÌÇÄò²¡ diabetes mellitus ¶þ±¶Ìå diploid DNA¸´ÖÆ DNA replication DNA²âÐò DNA sequencing ÏÔÐ﵀ dominant Ë«ÂÝÐý double helix ¸´ÖÆ duplication E µçÓ¾ electrophoresis Ellis - van Creveld syndrome ø enzyme ÍâÏÔ×Ó exon F ¼Ò×åÐÔµØÖк£ÈÈ familial Mediterranean fever Ó«¹âÔλÔÓ½» fluorescence in situ hybridization (FISH) ´àÐÔXȾɫÌå×ÛºÏÕ÷ Fragile X syndrome G »ùÒò gene »ùÒòÀ©Ôö gene amplification »ùÒò±í´ï gene expression »ùÒòͼÆ× gene mapping »ùÒò¿â gene pool »ùÒòÖÎÁÆ gene therapy »ùÒò×ªÒÆ gene transfer ÒÅ´«ÃÜÂë genetic code (ATGC) ÒÅ´«×Éѯ genetic counseling ÒÅ´«Í¼ genetic map ÒÅ´«±ê¼Ç genetic marker ÒÅ´«²¡É¸²é genetic screening »ùÒò×é genome »ùÒòÐÍ genotype ÖÖϵ germ line H µ¥±¶Ìå haploid haploinsufficiency ÔìѪ¸Éϸ°û hematopoietic stem cell ѪÓѲ¡ hemophilia ÔÓºÏ×Ó heterozygous ¸ß¶È±£ÊØÐòÁÐ highly conserved sequence Hirschsprung²¡ Hirschsprung's disease ´¿ºÏ×Ó homozygous È˹¤È¾É«Ìå human artificial chromosome (HAC) ÈËÀà»ùÒò×鼯»® Human Genome Project ÈËÀàÃâÒßȱÏݲ¡¶¾ human immunodeficiency virus (HIV)/ »ñµÃÐÔÃâÒßȱÏÝ×ÛºÏÕ÷ acquired immunodeficiency syndrome (AIDS) huntingtonÎ赸²¡ Huntington's disease ÔÓ½» hybridization I ÃâÒßÖÎÁÆ immunotherapy ÔλÔÓ½» in situ hybridization ¼Ì³ÐµÄ inherited ²åÈë insertion ֪ʶ²úȨ intellectual property rights K Çóý knockout L °×Ѫ²¡ leukemia ¿â library ¼ü¡¢Á¬½Ó linkage ²¿Î»¡¢³¡Ëù locus ÓÅÊÆ¶ÔÊýÆÀ·Ö LOD score ÁܰÍϸ°û lymphocyte M »ûÐÎ malformation Ãèͼ mapping ±ê¼Ç marker ºÚÉ«ËØÁö melanoma Ãϵ¶û Mendel, Johann (Gregor) Ãϵ¶ûÒÅ´« Mendelian inheritance ÐÅʹRNA messenger RNA (mRNA) [·ÖÁÑ]ÖÐÆÚ metaphase ΢Õó¼¼Êõ microarray technology ÏßÁ¢ÌåDNA mitochondrial DNA µ¥ÌåÐÔ monosomy СÊóÄ£ÐÍ mouse model ¶à·¢ÐÔÄÚ·ÖÃÚÁö²¡ multiple endocrine neoplasia, type 1 (MEN1) Í»±ä mutation N Éñ¾ÏËάÁö²¡ neurofibromatosis ÄáÂü-Ƥ¿Ë²¡ Niemann-Pick disease, type C (NPC) non-directiveness RNAÓ¡¼Ç Northern blot ºËÜÕËá nucleotide Éñ¾ºË nucleus O ¹ÑºËÜÕËá oligo °©»ùÒò oncogene P p53 Parkinson²¡ Parkinson's disease רÀûȨ patent Ѫϵ/Æ×ϵ pedigree ±íÐÍ phenotype ÎïÀíͼÆ× physical map ¶àÖ¸»ûÐÎ/¶àÖº»ûÐÎ polydactyly ¾ÛºÏøÁ´·´Ó¦ polymerase chain reaction (PCR) ¶à̬ÐÔ polymorphism ¶¨Î»¿Ë¡ positional cloning Ô·¢ÐÔÃâÒßȱÏÝ primary immunodeficiency ÒýÎï primer ÔºË pronucleus ǰÁÐÏÙ°© prostate cancer µ°°× protein R ÒþÐÔ recessive Äæ×ªÂ¼²¡¶¾ retrovirus ºËÌǺËËá ribonucleic acid (RNA) ºËÌÇÌå ribosome risk communication S ÐòÁбê¼Çλµã sequence-tagged site (STS) ÁªºÏÃâÒßȱÏÝ severe combined immunodeficiency (SCID) ÐÔȾɫÌå sex chromosome °éÐ﵀ sex-linked Ìåϸ°û somatic cells DNAÓ¡¼Ç Southern blot ¹âÆ×ºËÐÍ spectral karyotype (SKY) Ìæ´ú substitution ×Ôɱ»ùÒò suicide gene ×ÛºÏÕ÷ syndrome T ¼¼ÊõתÈà technology transfer ת»ùÒòµÄ transgenic Ò×λ translocation ÈýÌåÐÍ trisomy Ö×ÁöÒÖÖÆ»ùÒò tumor suppressor gene V ÔØÌå vector W µ°°×ÖÊÓ¡¼Ç Western blot Wolfram×ÛºÏÕ÷ Wolfram syndrome Y ½ÍĸÈ˹¤È¾É«Ìå yeast artificial chromosome (YAC) |
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