共 15 条
[1]
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region
[J].
Cruts, M
;
Rademakers, R
;
Gijselinck, I
;
van der Zee, J
;
Dermaut, B
;
de Pooter, T
;
de Rijk, P
;
Del-Favero, J
;
van Broeckhoven, C
.
HUMAN MOLECULAR GENETICS,
2005, 14 (13)
:1753-1762

Cruts, M
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium

Rademakers, R
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium

Gijselinck, I
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium

van der Zee, J
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium

Dermaut, B
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium

de Pooter, T
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium

论文数: 引用数:
h-index:
机构:

Del-Favero, J
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium

van Broeckhoven, C
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium Univ Antwerp VIB, Dept Mol Genet, Neurodegenerat Brain Dis Grp, B-2610 Antwerp, Belgium
[2]
Microduplication 22q11.2, an emerging syndrome: Clinical, cytogenetic, and molecular analysis of thirteen patients
[J].
Ensenauer, RE
;
Adeyinka, A
;
Flynn, HC
;
Michels, VV
;
Lindor, NM
;
Dawson, DB
;
Thorland, EC
;
Lorentz, CP
;
Goldstein, JL
;
McDonald, MT
;
Smith, WE
;
Simon-Fayard, E
;
Alexander, AA
;
Kulharya, AS
;
Ketterling, RP
;
Clark, RD
;
Jalal, SM
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2003, 73 (05)
:1027-1040

Ensenauer, RE
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Adeyinka, A
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Flynn, HC
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Michels, VV
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Lindor, NM
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Dawson, DB
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Thorland, EC
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Lorentz, CP
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Goldstein, JL
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

McDonald, MT
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Smith, WE
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Simon-Fayard, E
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Alexander, AA
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Kulharya, AS
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Ketterling, RP
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Clark, RD
论文数: 0 引用数: 0
h-index: 0
机构: Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA

Jalal, SM
论文数: 0 引用数: 0
h-index: 0
机构:
Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Cytogenet Lab, Rochester, MN 55905 USA
[3]
The tau H2 haplotype is almost exclusively Caucasian in origin
[J].
Evans, W
;
Fung, HC
;
Steele, J
;
Eerola, J
;
Tienari, P
;
Pittman, A
;
de Silva, R
;
Myers, A
;
Wavrant-De Vrieze, F
;
Singleton, A
;
Hardy, J
.
NEUROSCIENCE LETTERS,
2004, 369 (03)
:183-185

Evans, W
论文数: 0 引用数: 0
h-index: 0
机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA

Fung, HC
论文数: 0 引用数: 0
h-index: 0
机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA

Steele, J
论文数: 0 引用数: 0
h-index: 0
机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA

Eerola, J
论文数: 0 引用数: 0
h-index: 0
机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA

Tienari, P
论文数: 0 引用数: 0
h-index: 0
机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA

Pittman, A
论文数: 0 引用数: 0
h-index: 0
机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA

de Silva, R
论文数: 0 引用数: 0
h-index: 0
机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA

Myers, A
论文数: 0 引用数: 0
h-index: 0
机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA

Wavrant-De Vrieze, F
论文数: 0 引用数: 0
h-index: 0
机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA

Singleton, A
论文数: 0 引用数: 0
h-index: 0
机构: NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA

Hardy, J
论文数: 0 引用数: 0
h-index: 0
机构:
NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
[4]
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism
[J].
Koolen, David A.
;
Vissers, Lisenka E. L. M.
;
Pfundt, Rolph
;
de Leeuw, Nicole
;
Knight, Samantha J. L.
;
Regan, Regina
;
Kooy, R. Frank
;
Reyniers, Edwin
;
Romano, Corrado
;
Fichera, Marco
;
Schinzel, Albert
;
Baumer, Alessandra
;
Anderlid, Britt-Marie
;
Schoumans, Jacqueline
;
Knoers, Nine V.
;
van Kessel, Ad Geurts
;
Sistermans, Erik A.
;
Veltman, Joris A.
;
Brunner, Han G.
;
de Vries, Bert B. A.
.
NATURE GENETICS,
2006, 38 (09)
:999-1001

Koolen, David A.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Vissers, Lisenka E. L. M.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Pfundt, Rolph
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

de Leeuw, Nicole
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Knight, Samantha J. L.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Regan, Regina
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Kooy, R. Frank
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Reyniers, Edwin
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Romano, Corrado
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Fichera, Marco
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Schinzel, Albert
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Baumer, Alessandra
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Anderlid, Britt-Marie
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Schoumans, Jacqueline
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Knoers, Nine V.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

van Kessel, Ad Geurts
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Sistermans, Erik A.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Veltman, Joris A.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Brunner, Han G.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

de Vries, Bert B. A.
论文数: 0 引用数: 0
h-index: 0
机构:
Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
[5]
Lupski J.R., 2006, GENOMIC DISORDERS TH
[6]
DNA DUPLICATION ASSOCIATED WITH CHARCOT-MARIE-TOOTH DISEASE TYPE-1A
[J].
LUPSKI, JR
;
DEOCALUNA, RM
;
SLAUGENHAUPT, S
;
PENTAO, L
;
GUZZETTA, V
;
TRASK, BJ
;
SAUCEDOCARDENAS, O
;
BARKER, DF
;
KILLIAN, JM
;
GARCIA, CA
;
CHAKRAVARTI, A
;
PATEL, PI
.
CELL,
1991, 66 (02)
:219-232

LUPSKI, JR
论文数: 0 引用数: 0
h-index: 0
机构: BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX 77030

DEOCALUNA, RM
论文数: 0 引用数: 0
h-index: 0
机构: BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX 77030

SLAUGENHAUPT, S
论文数: 0 引用数: 0
h-index: 0
机构: BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX 77030

PENTAO, L
论文数: 0 引用数: 0
h-index: 0
机构: BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX 77030

GUZZETTA, V
论文数: 0 引用数: 0
h-index: 0
机构: BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX 77030

TRASK, BJ
论文数: 0 引用数: 0
h-index: 0
机构: BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX 77030

SAUCEDOCARDENAS, O
论文数: 0 引用数: 0
h-index: 0
机构: BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX 77030

BARKER, DF
论文数: 0 引用数: 0
h-index: 0
机构: BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX 77030

KILLIAN, JM
论文数: 0 引用数: 0
h-index: 0
机构: BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX 77030

GARCIA, CA
论文数: 0 引用数: 0
h-index: 0
机构: BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX 77030

CHAKRAVARTI, A
论文数: 0 引用数: 0
h-index: 0
机构: BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX 77030

PATEL, PI
论文数: 0 引用数: 0
h-index: 0
机构: BAYLOR UNIV,DEPT PEDIAT,HOUSTON,TX 77030
[7]
Molecular mechanism for duplication 17p11.2 - the homologous recombination reciprocal of the Smith-Magenis microdeletion
[J].
Potocki, L
;
Chen, KS
;
Park, SS
;
Osterholm, DE
;
Withers, MA
;
Kimonis, V
;
Summers, AM
;
Meschino, WS
;
Anyane-Yeboa, K
;
Kashork, CD
;
Shaffer, LG
;
Lupski, JR
.
NATURE GENETICS,
2000, 24 (01)
:84-87

Potocki, L
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Chen, KS
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Park, SS
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Osterholm, DE
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Withers, MA
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Kimonis, V
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Summers, AM
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Meschino, WS
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Anyane-Yeboa, K
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Kashork, CD
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Shaffer, LG
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

Lupski, JR
论文数: 0 引用数: 0
h-index: 0
机构:
Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[8]
APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy
[J].
Rovelet-Lecrux, A
;
Hannequin, D
;
Raux, G
;
Le Meur, N
;
Laquerrière, A
;
Vital, A
;
Dumanchin, C
;
Feuillette, S
;
Brice, A
;
Vercelletto, M
;
Dubas, F
;
Frebourg, T
;
Campion, D
.
NATURE GENETICS,
2006, 38 (01)
:24-26

Rovelet-Lecrux, A
论文数: 0 引用数: 0
h-index: 0
机构: INSERM, U614, IFRMP, Fac Med, Rouen, France

Hannequin, D
论文数: 0 引用数: 0
h-index: 0
机构: INSERM, U614, IFRMP, Fac Med, Rouen, France

Raux, G
论文数: 0 引用数: 0
h-index: 0
机构: INSERM, U614, IFRMP, Fac Med, Rouen, France

Le Meur, N
论文数: 0 引用数: 0
h-index: 0
机构: INSERM, U614, IFRMP, Fac Med, Rouen, France

Laquerrière, A
论文数: 0 引用数: 0
h-index: 0
机构: INSERM, U614, IFRMP, Fac Med, Rouen, France

Vital, A
论文数: 0 引用数: 0
h-index: 0
机构: INSERM, U614, IFRMP, Fac Med, Rouen, France

Dumanchin, C
论文数: 0 引用数: 0
h-index: 0
机构: INSERM, U614, IFRMP, Fac Med, Rouen, France

Feuillette, S
论文数: 0 引用数: 0
h-index: 0
机构: INSERM, U614, IFRMP, Fac Med, Rouen, France

Brice, A
论文数: 0 引用数: 0
h-index: 0
机构: INSERM, U614, IFRMP, Fac Med, Rouen, France

Vercelletto, M
论文数: 0 引用数: 0
h-index: 0
机构: INSERM, U614, IFRMP, Fac Med, Rouen, France

Dubas, F
论文数: 0 引用数: 0
h-index: 0
机构: INSERM, U614, IFRMP, Fac Med, Rouen, France

Frebourg, T
论文数: 0 引用数: 0
h-index: 0
机构: INSERM, U614, IFRMP, Fac Med, Rouen, France

Campion, D
论文数: 0 引用数: 0
h-index: 0
机构:
INSERM, U614, IFRMP, Fac Med, Rouen, France INSERM, U614, IFRMP, Fac Med, Rouen, France
[9]
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome
[J].
Sharp, Andrew J.
;
Hansen, Sierra
;
Selzer, Rebecca R.
;
Cheng, Ze
;
Regan, Regina
;
Hurst, Jane A.
;
Stewart, Helen
;
Price, Sue M.
;
Blair, Edward
;
Hennekam, Raoul C.
;
Fitzpatrick, Carrie A.
;
Segraves, Rick
;
Richmond, Todd A.
;
Guiver, Cheryl
;
Albertson, Donna G.
;
Pinkel, Daniel
;
Eis, Peggy S.
;
Schwartz, Stuart
;
Knight, Samantha J. L.
;
Eichler, Evan E.
.
NATURE GENETICS,
2006, 38 (09)
:1038-1042

Sharp, Andrew J.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA

Hansen, Sierra
论文数: 0 引用数: 0
h-index: 0
机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA

Selzer, Rebecca R.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA

Cheng, Ze
论文数: 0 引用数: 0
h-index: 0
机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA

Regan, Regina
论文数: 0 引用数: 0
h-index: 0
机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA

Hurst, Jane A.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA

Stewart, Helen
论文数: 0 引用数: 0
h-index: 0
机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA

Price, Sue M.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA

Blair, Edward
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机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA

Hennekam, Raoul C.
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Fitzpatrick, Carrie A.
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Segraves, Rick
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Richmond, Todd A.
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Guiver, Cheryl
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Albertson, Donna G.
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机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA

Pinkel, Daniel
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机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA

Eis, Peggy S.
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Schwartz, Stuart
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Knight, Samantha J. L.
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Eichler, Evan E.
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机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA
[10]
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability
[J].
Shaw-Smith, Charles
;
Pittman, Alan M.
;
Willatt, Lionel
;
Martin, Howard
;
Rickman, Lisa
;
Gribble, Susan
;
Curley, Rebecca
;
Cumming, Sally
;
Dunn, Carolyn
;
Kalaitzopoulos, Dimitrios
;
Porter, Keith
;
Prigmore, Elena
;
Krepischi-Santos, Ana C. V.
;
Varela, Monica C.
;
Koiffmann, Celia P.
;
Lees, Andrew J.
;
Rosenberg, Carla
;
Firth, Helen V.
;
de Silva, Rohan
;
Carter, Nigel P.
.
NATURE GENETICS,
2006, 38 (09)
:1032-1037

Shaw-Smith, Charles
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h-index: 0
机构:
Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Pittman, Alan M.
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Willatt, Lionel
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Martin, Howard
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Rickman, Lisa
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Gribble, Susan
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Curley, Rebecca
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Cumming, Sally
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Dunn, Carolyn
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Kalaitzopoulos, Dimitrios
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Porter, Keith
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机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Prigmore, Elena
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Krepischi-Santos, Ana C. V.
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Varela, Monica C.
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Koiffmann, Celia P.
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Lees, Andrew J.
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Rosenberg, Carla
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机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Firth, Helen V.
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

de Silva, Rohan
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England

Carter, Nigel P.
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h-index: 0
机构: Univ Cambridge, Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 2QQ, England