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20篇 您的检索式：作者名="Herbrick"

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	题名	作者	年代	出处	被引量
1	Molecular analysis of the PDS gene in pendred syndrome显示文摘	Coyle B Reardon W Herbrick JA	1998	Hum Mol Genet1998，7，：	1
2	Molecular analysis of the PDS gene in Pendred syndrome显示文摘	Coyle B Reardon W Herbrick JA	1998	Hum Mol Genet1998，71，105：	1
3	Molecular analysis of the PDS gene in Pendred syndrome显示文摘	Coyle/3 Reardon W Herbrick JA	1998	Hum Mol Genet1998，7，：	1
4	Molecular analysis of the PDS gene in Pendred syndrome (sensorineural hearing loss and goitre)显示文摘	Oyle B Reardon W Herbrick JA	1998	Human Molecular Genetics1998，7，：	1
5	Molecular analysis of the PDS gene in Pendred syndrome(sensorineural hearing loss and goitre)显示文摘	Coyle B Reardon W Herbrick JA	1998	Human Molecular Genetics1998，7，：	1
6	Molecular analysis of the PDS gene in Pendred syndrome (sensorineural hearing loss and goitre) 显示文摘	Coyle B Reardon W Herbrick JA	1998	Human Molecular Genetics1998，7，：	1
7	Molecular analysis of the PDS gene in Pendred syndrome显示文摘	Coyle B Reardon W Herbrick J A	1998	Hum Mol Genet1998，7，：	1
8	Holo- prosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations: case report and review of the literature显示文摘	Fernandez BA Siegel-Bartelt J Herbrick JA	2005	Clin Genet2005，68，4：	1
9	Structural characterization and mapping of the normal epithelial cell-specificl gene 显示文摘	Luo L Herbrick JA Scherer SW	1998	Bio- chem Biophys Res Commun1998，247，3：	1
10	Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual显示文摘	Vincent JB Herbrick JA Gurling HM	2000	Am J Hum Genet2000，67，2：	1
11	Molecular analysis of the PDS gene in Pendred syndrome显示文摘	Coyle B Reardon W Herbrick JA	1998	Hum Mol Genet1998，7，：	1
12	Molecular analysis of the SLC26A4 gene in Pendred syndrome显示文摘	Coyle B Reardon W Herbrick JA	1998	Hum Mol Genet1998，7，：	1
13	Structural characterization and mapping of the normal epithelial cellspecific 1 gene显示文摘	Herbrick JA Scherer SW	1998	Biochem Biophys Res Commun1998，247，3：	1
14	Molecular analysis of the PDS gene in Pendred syndrome显示文摘	Coyle B Reardon W Herbrick JA	1998	Hum Mol Genet1998，7，：	1
15	Structural characterization and mapping of the normal epithelial cellspecific 1 gene显示文摘	Luo L Herbrick JA Scherer SW	1998	Biochem Biophys Res Commun1998，247，3：	1
16	Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual显示文摘	Vincent J B Herbrick J A Gurling H M	2000	Am J Hum Genet2000，67，2：	1
17	Structural characterization and mapping of the normal epithelial cell-specific 1 gene显示文摘	Luo L Herbrick JA Scherer SW	1998	Biochem Biophys Res Commun1998，247，3：	1
18	Structural characterization and mapping of the normal epithelial cell-specific 1 gene显示文摘	LUO L HERBRICK J A SCHERER S W	1998	Biochem Biophys Res Commun1998，247，3：	1
19	Holoprosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations:Case report and review of the literature显示文摘	Fernandez BA Siegel-Bartelt J Herbrick JA		0，，04：	1
20	Structural characterization and mapping of the normal epithelial cell-specific 1 gene显示文摘	Luo L Herbrick JA Scherer SW	1998	Biochem Biophys Res Commun1998，247，3：	1

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