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45篇 您的检索式：作者名="KELSELL DP"

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	题名	作者	年代	出处	被引量
1	Cornexin 26 mutations in hereditary non-syndromic sensorineural deafness显示文摘	Kelsell DP Dunlop J Stevens HP		0，，6628：	1
2	Linkage of monilethrix to the triehocyte and epithelial keratin gene cluster on 12q11 - q13 显示文摘	Stevens HP Kelsell DP Bryant SP	1996	J Invest Dermatol1996，106，4：	1
3	Connexin 26 mutations in hereditary nonsyndromic sensorineural deafness显示文摘	Kelsell DP Dunlop J Stevens HP	1997	Nature1997，387，：	1
4	Localization of a second NM23 gene,NME2,tochromosome 17q21-q22显示文摘	Kelsell DP Black DM Solomon E	1993	Genomics1993，17，2：	1
5	Connexin 26 mutations in hereditary nonsynsdrome sensorineural deafness显示文摘	Kelsell DP Dunlop J Stevens HP	1997	Nature1997，387，：	1
6	The palmoplantar keratodermas:much more than palms and soles显示文摘	Kelsell DP Stevens HP		0，，：	1
7	Connexin 26 mutations in hereditary non-syndromic sensorineural deafness显示文摘	Kelsell DP Dunlop J Stevens HP	1997	Nature1997，387，：	1
8	Punctate palmoplantar keratoderma and malignancy in a fourgeneration family显示文摘	Stevens HP Kelsell DP Leigh IM	1996	Br J Dermatol1996，134，：	1
9	Genetic linkage studies in non-epidermolytic palmoplantar keratoderma:evidence for heterogeneity显示文摘	Kelsell DP Stevens HP Ratnavel R	1995	Hum Mol Genet1995，4，：	1
10	Connexin 26 mutations in hereditary non-syndromic sensorineural deafness显示文摘	Kelsell DP Dunlop J Stevens HP	1997	Nature1997，387，：	1
11	Cell - cell connectivity : Desrao-somes and disease 显示文摘	Brooke MA Nitoiu D Kelsell DP	2012	J Pathol2012，226，2：	1
12	Connexin 26 mutations inhereditary nonsyndromic sensorineural deafness显示文摘	Kelsell DP Dunlop J Stevens HP	1997	Nature1997，387，6628：	1
13	Connexin 26 mutation in heredity non-syndromic sensorineural deafness显示文摘	KELSELL DP DUNLOP J STEVEN HP	1997	Nature1997，387，：	1
14	Key functions for gap junctions in skin and hearing显示文摘	Scott CA Kelsell DP	2011	Biochem J2011，438，：	1
15	Connexin26 mutations inhereditary nonsyndromie sensorineural deafness显示文摘	Kelsell DP Dunlop J Stevens HP	1997	Nature1997，387，：	1
16	Human diseases: clues to cracking the connexin code 显示文摘	Kelsell DP Dunlop J Hodgins MB	2001	Trends in cell biology2001，11，1：	1
17	Connexin 26 mutations in he- reditary non - syndromic sensorineural deafness 显示文摘	Kelsell DP Dunlop J Stevens HP	1997	Nature1997，387，6628：	1
18	Connexin 26 mutations in hereditary non-syndromic sensorineural deafness显示文摘	Kelsell DP Dunlop J Stevens HP	1997	Nature1997，387，6628：	1
19	Genetic analysis of the BRCA1 region in a large breast/ovarian family:refinement of the minimal region containing BRCA 1显示文摘	KELSELL DP BLACK DM BISHOP DT	1993	Hum Mol Genet1993，2，：	1
20	Mutational analysis of selected genes in the TGF beta, Wnt, pRb, and p53 pathways in primary uveal melanoma显示文摘	Edmunds SC Kelsell DP Hungerford JL	2002	Invest Ophthalmol Vis Sci2002，43，：	1

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