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20篇 您的检索式：作者名="Spinner NB"

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	题名	作者	年代	出处	被引量
1	Renal involvement and the role of Notch signalling in Alagille syndrome显示文摘	Kamath BM Spinner NB Rosenblum ND	2013	Nat Rev Nephrol2013，9，7：	1
2	Infantile spasms associated with proximal duplication of chromosome 15q显示文摘	Bingham PM Spinner NB Sovinsky L	1996	PediatrNeurol1996，15，2：	1
3	Notch signaling in human development and disease显示文摘	Penton AL Leonard LD Spinner NB	2012	Semin Cell Dev Biol2012，23，4：	1
4	Jaggedl (JAG1): Structure, expression, and disease associations显示文摘	Grochowski CM Loomes KM Spinner NB	2016	Gene2016，576，13：	1
5	Clinical and molecular genetics of Alagille syndrome显示文摘	Krantz ID Piccoli DA Spinner NB	1999	Curr Opin Pediatr1999，11，6：	1
6	Notch signaling in human development and disease显示文摘	Penton AL Leonard LD Spinner NB	2012	Semin Cell Dev Biol2012，23，4：	1
7	Monozygotic twins with a severe form of Alagille syndrome and phenotypic discordance显示文摘	Kamath BM Krantz ID Spinner NB	2002	Am J Med Genet2002，112，2：	1
8	Alagille syndrome and the Jaggedl gene 显示文摘	Pieeoli DA Spinner NB	2001	Semin Liver Dis2001，21，4：	1
9	Notch signaling in human development and disease显示文摘	Penton AL Leonard LD Spinner NB		0，，：	1
10	Notch signaling in human development and disease 显示文摘	Penton AL Leonard LD Spinner NB	2012	Semin Cell Dev Biol2012，23，4：	1
11	Alagille syndrome and the Jaggedl gene显示文摘	Piccoli DA Spinner NB	2001	Semin Liver Dis2001，21，4：	1
12	Notch signaling in humandevelopment and disease显示文摘	Penton AL Leonard LD Spinner NB	2012	Seminars Cell Dev Bio2012，23，4：	1
13	Notch signaling in human development and disease显示文摘	Penton AL Leonard LD Spinner NB		0，，04：	1
14	Alagille syndrome and the Jagged 1 gene显示文摘	Piccoli DA Spinner NB	2001	SeminLiverDis2001，21，4：	1
15	Vascular anomalies in Alagille syndrome:a significant cause of morbidity and mortality显示文摘	Kamath BM Spinner NB Emerick KM	2004	Circulation2004，109，11：	1
16	Alagilie syndrome and the Jagged 1 gene显示文摘	Piceoli DA Spinner NB	2001	Semin Liver Dis2001，21，52：	1
17	Notch signaling in human development and disease显示文摘	Penton AL Leonard LD Spinner NB	2012	Semin Cell Dev Biol2012，23，4：	1
18	Genome-wide SNP geno-typing identifies the Stereocilin (STRC) gene as a major contribu-tor to pediatric bilateral sensorineural hearing impairment显示文摘	Francey LJ Conlin LK Kadesch HE Clark D Berrodin D Sun Y Glessner J Hakonarson H Jalas C Landau C Spinner NB Kenna M Sagi M Rehm HL Krantz ID		0，，02：	1
19	Notch signaling in human development and disease显示文摘	Penton AL Leonard LD Spinner NB		0，，04：	1
20	Notch signaling in human development and disease显示文摘	Penton AL Leonard LD Spinner NB	2012	Semin Cell Dev Biol2012，23，4：	1

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