共 45 条
[1]
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
[J].
Ahmed, ZM
;
Riazuddin, S
;
Bernstein, SL
;
Ahmed, Z
;
Khan, S
;
Griffith, AJ
;
Morell, RJ
;
Friedman, TB
;
Riazuddin, S
;
Wilcox, ER
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2001, 69 (01)
:25-34

Ahmed, ZM
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Genet Mol Lab, NIH, Rockville, MD 20850 USA

Riazuddin, S
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Genet Mol Lab, NIH, Rockville, MD 20850 USA

Bernstein, SL
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Genet Mol Lab, NIH, Rockville, MD 20850 USA

论文数: 引用数:
h-index:
机构:

Khan, S
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Genet Mol Lab, NIH, Rockville, MD 20850 USA

Griffith, AJ
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Genet Mol Lab, NIH, Rockville, MD 20850 USA

Morell, RJ
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Genet Mol Lab, NIH, Rockville, MD 20850 USA

Friedman, TB
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Genet Mol Lab, NIH, Rockville, MD 20850 USA

Riazuddin, S
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Genet Mol Lab, NIH, Rockville, MD 20850 USA

Wilcox, ER
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Genet Mol Lab, NIH, Rockville, MD 20850 USA
[2]
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
[J].
Alagramam, KN
;
Yuan, HJ
;
Kuehn, MH
;
Murcia, CL
;
Wayne, S
;
Srisailpathy, CRS
;
Lowry, RB
;
Knaus, R
;
Van Laer, L
;
Bernier, FP
;
Schwartz, S
;
Lee, C
;
Morton, CC
;
Mullins, RF
;
Ramesh, A
;
Van Camp, G
;
Hagemen, GS
;
Woychik, RP
;
Smith, RJH
.
HUMAN MOLECULAR GENETICS,
2001, 10 (16)
:1709-1718

Alagramam, KN
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

Yuan, HJ
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

Kuehn, MH
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

Murcia, CL
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

Wayne, S
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

Srisailpathy, CRS
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

Lowry, RB
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

Knaus, R
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

论文数: 引用数:
h-index:
机构:

Bernier, FP
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

论文数: 引用数:
h-index:
机构:

Lee, C
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

Morton, CC
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

Mullins, RF
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

Ramesh, A
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

论文数: 引用数:
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Hagemen, GS
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

Woychik, RP
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA

Smith, RJH
论文数: 0 引用数: 0
h-index: 0
机构:
Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA Case Western Reserve Univ, Univ Hosp Cleveland, Rainbow Babies & Childrens Hosp, Dept Pediat, Cleveland, OH 44106 USA
[3]
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
[J].
Alagramam, KN
;
Murcia, CL
;
Kwon, HY
;
Pawlowski, KS
;
Wright, CG
;
Woychik, RP
.
NATURE GENETICS,
2001, 27 (01)
:99-102

Alagramam, KN
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA

Murcia, CL
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA

Kwon, HY
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA

Pawlowski, KS
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA

Wright, CG
论文数: 0 引用数: 0
h-index: 0
机构: Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA

Woychik, RP
论文数: 0 引用数: 0
h-index: 0
机构:
Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA Case Western Reserve Univ, Dept Pediat, Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
[4]
Angst BD, 2001, J CELL SCI, V114, P625
[5]
A millennial myosin census
[J].
Berg, JS
;
Powell, BC
;
Cheney, RE
.
MOLECULAR BIOLOGY OF THE CELL,
2001, 12 (04)
:780-794

Berg, JS
论文数: 0 引用数: 0
h-index: 0
机构:
Univ N Carolina, Dept Cell & Mol Physiol, Chapel Hill, NC 27599 USA Univ N Carolina, Dept Cell & Mol Physiol, Chapel Hill, NC 27599 USA

Powell, BC
论文数: 0 引用数: 0
h-index: 0
机构:
Univ N Carolina, Dept Cell & Mol Physiol, Chapel Hill, NC 27599 USA Univ N Carolina, Dept Cell & Mol Physiol, Chapel Hill, NC 27599 USA

Cheney, RE
论文数: 0 引用数: 0
h-index: 0
机构:
Univ N Carolina, Dept Cell & Mol Physiol, Chapel Hill, NC 27599 USA Univ N Carolina, Dept Cell & Mol Physiol, Chapel Hill, NC 27599 USA
[6]
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
[J].
Bitner-Glindzicz, M
;
Lindley, KJ
;
Rutland, P
;
Blaydon, D
;
Smith, VV
;
Milla, PJ
;
Hussain, K
;
Furth-Lavi, J
;
Cosgrove, KE
;
Shepherd, RM
;
Barnes, PD
;
O'Brien, RE
;
Farndon, PA
;
Sowden, J
;
Liu, XZ
;
Scanlan, MJ
;
Malcolm, S
;
Dunne, MJ
;
Aynsley-Green, A
;
Glaser, B
.
NATURE GENETICS,
2000, 26 (01)
:56-60

Bitner-Glindzicz, M
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Lindley, KJ
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Rutland, P
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Blaydon, D
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Smith, VV
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Milla, PJ
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Hussain, K
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Furth-Lavi, J
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Cosgrove, KE
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Shepherd, RM
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Barnes, PD
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

O'Brien, RE
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Farndon, PA
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Sowden, J
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Liu, XZ
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Scanlan, MJ
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Malcolm, S
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Dunne, MJ
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Aynsley-Green, A
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England

Glaser, B
论文数: 0 引用数: 0
h-index: 0
机构: Inst Child Hlth, Dept Clin & Mol Genet, London, England
[7]
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
[J].
Bolz, H
;
von Brederlow, B
;
Ramírez, A
;
Bryda, EC
;
Kutsche, K
;
Nothwang, HG
;
Seeliger, M
;
Cabrera, MDS
;
Vila, MC
;
Molina, OP
;
Gal, A
;
Kubisch, C
.
NATURE GENETICS,
2001, 27 (01)
:108-112

Bolz, H
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany

von Brederlow, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany

Ramírez, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany

Bryda, EC
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany

Kutsche, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany

Nothwang, HG
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany

Seeliger, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany

Cabrera, MDS
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany

Vila, MC
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany

Molina, OP
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany

Gal, A
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany

Kubisch, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hamburg, Krankenhaus Eppendorf, Inst Human Genet, D-2000 Hamburg, Germany
[8]
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
[J].
Bork, JM
;
Peters, LM
;
Riazuddin, S
;
Bernstein, SL
;
Ahmed, ZM
;
Ness, SL
;
Polomeno, R
;
Ramesh, A
;
Schloss, M
;
Srisailpathy, CRS
;
Wayne, S
;
Bellman, S
;
Desmukh, D
;
Ahmed, Z
;
Khan, SN
;
Kaloustian, VMD
;
Li, XC
;
Lalwani, A
;
Riazuddin, S
;
Bitner-Glindzicz, M
;
Nance, WE
;
Liu, XZ
;
Wistow, G
;
Smith, RJH
;
Griffith, AJ
;
Wilcox, ER
;
Friedman, TB
;
Morell, RJ
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2001, 68 (01)
:26-37

Bork, JM
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Peters, LM
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Riazuddin, S
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Bernstein, SL
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Ahmed, ZM
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Ness, SL
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Polomeno, R
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Ramesh, A
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Schloss, M
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Srisailpathy, CRS
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Wayne, S
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Bellman, S
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Desmukh, D
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Ahmed, Z
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Khan, SN
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Kaloustian, VMD
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Li, XC
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Lalwani, A
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Riazuddin, S
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Bitner-Glindzicz, M
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Nance, WE
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Liu, XZ
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Wistow, G
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Smith, RJH
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Griffith, AJ
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Wilcox, ER
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Friedman, TB
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA

Morell, RJ
论文数: 0 引用数: 0
h-index: 0
机构: Natl Inst Deafness & Other Commun Disorders, Mol Genet Lab, NIH, Rockville, MD 20850 USA
[9]
Cox B, 2000, DEV DYNAM, V217, P233, DOI 10.1002/(SICI)1097-0177(200003)217:3<233::AID-DVDY1>3.0.CO
[10]
2-O
