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23篇 您的检索式：期刊名="AmJHumGenet"

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	题名	作者	年代	出处	被引量
1	Construction of a ge- netic linkage map using restriction fragment length polymorphisms 显示文摘	Botsein D White R L Skolnick M	1980	AmJHumGenet1980，32，3：	1
2	Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement 显示文摘	Kobayashi H Abe K Matsuura T	2011	AmJHumGenet2011，89，1：	1
3	PLINK: a tool set for whole - genome association and population - based linkage analyses 显示文摘	S Purcell B Neale K Todd -Brown	2007	AmJHumGenet2007，81，3：	1
4	Construction of a genetic linkage map in man using restriction fragment length polymorphisms 显示文摘	Botstein D White R L Skolnick M	1980	AmJHumGenet1980，32，：	1
5	GeneticlinkagemapofsixpolymorphicDNAmarkersaroundthegeneforfamilialadenomatouspolyposisofchromosome5显示文摘	DunlopMG WyllieAH NakamuraY etal	1990	AmJHumGenet1990，47，5：	1
6	Associationofthegeneencodingwingless-typemammarytumorvirusintegration-sitefamilymember5B(WNT5B)withtype2diabetes显示文摘	KanazawaA TsukadaS SekineA etal	2004	AmJHumGenet2004，75，5：	1
7	Construction of a genetic linkage map in man using restriction fragment length polymorhisns 显示文摘	Botstenin D White RL Skolnich M	1980	AmJHumGenet1980，32，：	1
8	Linkageofavariantorattenuatedformofadenomatouspolyposiscolitotheadenomatouspolyposiscoli(APC)locus显示文摘	SpriioL OtterudB StaufferD etal	1992	AmJHumGenet1992，51，6：	1
9	Shifting paradigm of association studies : value of rare single-nucleotide polymorphisms 显示文摘	Gorlov IP Gorlova OY Sunyaev SR	2008	AmJHumGenet2008，82，1：	1
10	Construction of a genetic linkage map in man using restriction fragment length polymorphisms 显示文摘	Botstein D White R L Skolnick M	1980	AmJHumGenet1980，32，：	1
11	Constltudveiy methyla- ted CpG dinucleotides as mutation hot spots in the retinoblastoma gene (RB1) 显示文摘	Mancini D Singh S Ainsworth P	1997	AmJHumGenet1997，61，1：	1
12	Heteroplasmic point mutations in the human mtDNA control region 显示文摘	Bendall KE Macaulay VA Baker JR	1996	AmJHumGenet1996，59，6：	1
13	ASecondlocusforRiegersyndromemapstochromosome13q14显示文摘	3,PhillipsJC DelBonoE HainesJ etal	1996	AmJHumGenet1996，59，：	1
14	Five years of GWASdiscovery 显示文摘	Visscher PM Brown MA Mccarthy MI	2012	AmJHumGenet2012，90，1：	1
15	Novel vitiligo suscepti- bility loci on chromosomes 7 ( AIS2 ) and 8 ( AIS3 ) , confirmation of SLEV1 on chromosome 17, and their roles in an autoimmune di- athesis 显示文摘	Spritz RA Gowan K Bennett DC	2004	AmJHumGenet2004，74，1：	1
16	Evaluation of 13 short tandem repeat loci for use in personal identification applications 显示文摘	Jin L Zhong Y	1994	AmJHumGenet1994，55，：	1
17	Evidence that alocus for familial high myopia maps to chromosome 18p 显示文摘	YOUNG TL RONAN SM DRAHOZAL LA	1998	AmJHumGenet1998，63，1：	1
18	Multiple Genes for essentialhypertension susceptibility on chromosome 1 q 显示文摘	Chang YP Liu X Kim JD	2007	AmJHumGenet2007，80，2：	1
19	Mutationalanalysisofpatientswithneurofibromatosis2显示文摘	MacCollinM RameshV JacobyLB etal	1994	AmJHumGenet1994，55，2：	1
20	Typeofmutationintheneurofibromatosistype2gene(NF2)frequentlydeterminesseverityofdiseases显示文摘	RuttledgeMH AndermannAA PhelanCM etal	1996	AmJHumGenet1996，59，2：	1

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