共 478 条
[1]
Mutations in NSUN2 Cause Autosomal-Recessive Intellectual Disability
[J].
Abbasi-Moheb, Lia
;
Mertel, Sara
;
Gonsior, Melanie
;
Nouri-Vahid, Leyla
;
Kahrizi, Kimia
;
Cirak, Sebahattin
;
Wieczorek, Dagmar
;
Motazacker, M. Mahdi
;
Esmaeeli-Nieh, Sahar
;
Cremer, Kirsten
;
Weissmann, Robert
;
Tzschach, Andreas
;
Garshasbi, Masoud
;
Abedini, Seyedeh S.
;
Najmabadi, Hossein
;
Ropers, H. Hilger
;
Sigrist, Stephan J.
;
Kuss, Andreas W.
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2012, 90 (05)
:847-855

Abbasi-Moheb, Lia
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Mol Genet, D-14195 Berlin, Germany
Univ Social Welf & Rehabil Sci, Genet Res Ctr, Tehran 1985713834, Iran Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Mertel, Sara
论文数: 0 引用数: 0
h-index: 0
机构:
Free Univ Berlin, Inst Biol Genet, D-14195 Berlin, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Gonsior, Melanie
论文数: 0 引用数: 0
h-index: 0
机构:
Free Univ Berlin, Inst Biol Genet, D-14195 Berlin, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Nouri-Vahid, Leyla
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Social Welf & Rehabil Sci, Genet Res Ctr, Tehran 1985713834, Iran Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Kahrizi, Kimia
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Social Welf & Rehabil Sci, Genet Res Ctr, Tehran 1985713834, Iran Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Cirak, Sebahattin
论文数: 0 引用数: 0
h-index: 0
机构:
Great Ormond St Childrens Hosp, Inst Child Hlth, London WC1N 1EH, England Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Wieczorek, Dagmar
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Klinikum Essen, Inst Humangenet, D-45147 Essen, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Motazacker, M. Mahdi
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Mol Genet, D-14195 Berlin, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Esmaeeli-Nieh, Sahar
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Mol Genet, D-14195 Berlin, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Cremer, Kirsten
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Klinikum Essen, Inst Humangenet, D-45147 Essen, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Weissmann, Robert
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Med Greifswald, Inst Human Genet, D-17489 Greifswald, Germany
Univ Greifswald, Interfac Inst Genet & Funct Genom, D-17489 Greifswald, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Tzschach, Andreas
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Mol Genet, D-14195 Berlin, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Garshasbi, Masoud
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Mol Genet, D-14195 Berlin, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Abedini, Seyedeh S.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Social Welf & Rehabil Sci, Genet Res Ctr, Tehran 1985713834, Iran Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Najmabadi, Hossein
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Social Welf & Rehabil Sci, Genet Res Ctr, Tehran 1985713834, Iran Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Ropers, H. Hilger
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Mol Genet, D-14195 Berlin, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Sigrist, Stephan J.
论文数: 0 引用数: 0
h-index: 0
机构:
Free Univ Berlin, Inst Biol Genet, D-14195 Berlin, Germany
Charite, NeuroCure Cluster Excellence, D-10117 Berlin, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany

Kuss, Andreas W.
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Mol Genet, D-14195 Berlin, Germany
Univ Med Greifswald, Inst Human Genet, D-17489 Greifswald, Germany
Univ Greifswald, Interfac Inst Genet & Funct Genom, D-17489 Greifswald, Germany Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[2]
RNA, helicases: Regulators of differentiation
[J].
Abdelhaleem, M
.
CLINICAL BIOCHEMISTRY,
2005, 38 (06)
:499-503

Abdelhaleem, M
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Toronto, Hosp Sick Children, Dept Paediat Lab Med, Div Haematopathol, Toronto, ON M5G 1X8, Canada Univ Toronto, Hosp Sick Children, Dept Paediat Lab Med, Div Haematopathol, Toronto, ON M5G 1X8, Canada
[3]
Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3
[J].
Abreu, Ana Paula
;
Dauber, Andrew
;
Macedo, Delanie B.
;
Noel, Sekoni D.
;
Brito, Vinicius N.
;
Gill, John C.
;
Cukier, Priscilla
;
Thompson, Iain R.
;
Navarro, Victor M.
;
Gagliardi, Priscila C.
;
Rodrigues, Tania
;
Kochi, Cristiane
;
Longui, Carlos Alberto
;
Beckers, Dominique
;
de Zegher, Francis
;
Montenegro, Luciana R.
;
Mendonca, Berenice B.
;
Carroll, Rona S.
;
Hirschhorn, Joel N.
;
Latronico, Ana Claudia
;
Kaiser, Ursula B.
.
NEW ENGLAND JOURNAL OF MEDICINE,
2013, 368 (26)
:2467-2475

Abreu, Ana Paula
论文数: 0 引用数: 0
h-index: 0
机构:
Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA
Univ Sao Paulo, Fac Med, Hosp Clin,Lab Hormonios & Genet Mol,LIM42, Disciplina Endocrinol,Unidade Endocrinol Desenvol, BR-05403900 Sao Paulo, Brazil Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Dauber, Andrew
论文数: 0 引用数: 0
h-index: 0
机构:
Boston Childrens Hosp, Div Endocrinol, Boston, MA USA
Broad Inst, Program Med & Populat Genet, Cambridge, MA USA Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Macedo, Delanie B.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sao Paulo, Fac Med, Hosp Clin,Lab Hormonios & Genet Mol,LIM42, Disciplina Endocrinol,Unidade Endocrinol Desenvol, BR-05403900 Sao Paulo, Brazil Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Noel, Sekoni D.
论文数: 0 引用数: 0
h-index: 0
机构:
Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Brito, Vinicius N.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sao Paulo, Fac Med, Hosp Clin,Lab Hormonios & Genet Mol,LIM42, Disciplina Endocrinol,Unidade Endocrinol Desenvol, BR-05403900 Sao Paulo, Brazil Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Gill, John C.
论文数: 0 引用数: 0
h-index: 0
机构:
Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Cukier, Priscilla
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sao Paulo, Fac Med, Hosp Clin,Lab Hormonios & Genet Mol,LIM42, Disciplina Endocrinol,Unidade Endocrinol Desenvol, BR-05403900 Sao Paulo, Brazil Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Thompson, Iain R.
论文数: 0 引用数: 0
h-index: 0
机构:
Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Navarro, Victor M.
论文数: 0 引用数: 0
h-index: 0
机构:
Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Gagliardi, Priscila C.
论文数: 0 引用数: 0
h-index: 0
机构:
Nemours Childrens Clin, Div Endocrinol Diabet & Metab, Jacksonville, FL USA Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Rodrigues, Tania
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Fed Minas Gerais, Hosp Clin, Div Pediat Endocrinol, Belo Horizonte, MG, Brazil Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Kochi, Cristiane
论文数: 0 引用数: 0
h-index: 0
机构:
Fac Ciencias Med Santa Casa Sao Paulo, Dept Pediat, Sao Paulo, Brazil Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Longui, Carlos Alberto
论文数: 0 引用数: 0
h-index: 0
机构:
Fac Ciencias Med Santa Casa Sao Paulo, Dept Pediat, Sao Paulo, Brazil Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Beckers, Dominique
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Hosp Gasthuisberg, Dept Pediat, B-3000 Louvain, Belgium Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

de Zegher, Francis
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Hosp Gasthuisberg, Dept Pediat, B-3000 Louvain, Belgium Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Montenegro, Luciana R.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sao Paulo, Fac Med, Hosp Clin,Lab Hormonios & Genet Mol,LIM42, Disciplina Endocrinol,Unidade Endocrinol Desenvol, BR-05403900 Sao Paulo, Brazil Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Mendonca, Berenice B.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sao Paulo, Fac Med, Hosp Clin,Lab Hormonios & Genet Mol,LIM42, Disciplina Endocrinol,Unidade Endocrinol Desenvol, BR-05403900 Sao Paulo, Brazil Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Carroll, Rona S.
论文数: 0 引用数: 0
h-index: 0
机构:
Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Hirschhorn, Joel N.
论文数: 0 引用数: 0
h-index: 0
机构:
Boston Childrens Hosp, Div Endocrinol, Boston, MA USA
Boston Childrens Hosp, Div Genet, Boston, MA USA
Broad Inst, Program Med & Populat Genet, Cambridge, MA USA Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Latronico, Ana Claudia
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sao Paulo, Fac Med, Hosp Clin,Lab Hormonios & Genet Mol,LIM42, Disciplina Endocrinol,Unidade Endocrinol Desenvol, BR-05403900 Sao Paulo, Brazil Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA

Kaiser, Ursula B.
论文数: 0 引用数: 0
h-index: 0
机构:
Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USA Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA 02115 USA
[4]
The Sm domain is an ancient RNA-binding motif with oligo(U) specificity
[J].
Achsel, T
;
Stark, H
;
Lührmann, R
.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
2001, 98 (07)
:3685-3689

Achsel, T
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany

Stark, H
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany

Lührmann, R
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
[5]
Mutations Disrupting Selenocysteine Formation Cause Progressive Cerebello-Cerebral Atrophy
[J].
Agamy, Orly
;
Ben Zeev, Bruria
;
Lev, Dorit
;
Marcus, Barak
;
Fine, Dina
;
Su, Dan
;
Narkis, Ginat
;
Ofir, Rivka
;
Hoffmann, Chen
;
Leshinsky-Silver, Esther
;
Flusser, Hagit
;
Sivan, Sara
;
Soll, Dieter
;
Lerman-Sagie, Tally
;
Birk, Ohad S.
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2010, 87 (04)
:538-544

Agamy, Orly
论文数: 0 引用数: 0
h-index: 0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel

Ben Zeev, Bruria
论文数: 0 引用数: 0
h-index: 0
机构:
Chaim Sheba Med Ctr, Pediat Neurol Unit, Ramat Gan, Israel
Chaim Sheba Med Ctr, Dept Diagnost Imaging, Ramat Gan, Israel Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel

Lev, Dorit
论文数: 0 引用数: 0
h-index: 0
机构:
Wolfson Med Ctr, Inst Med Genet, Holon, Israel
Wolfson Med Ctr, Pediat Neurol Unit, Holon, Israel Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel

论文数: 引用数:
h-index:
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Fine, Dina
论文数: 0 引用数: 0
h-index: 0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel

Su, Dan
论文数: 0 引用数: 0
h-index: 0
机构:
Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT USA
Yale Univ, Dept Chem, New Haven, CT USA Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel

Narkis, Ginat
论文数: 0 引用数: 0
h-index: 0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel
Soroka Univ, Med Ctr, Genet Inst, Beer Sheva, Israel Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel

论文数: 引用数:
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Hoffmann, Chen
论文数: 0 引用数: 0
h-index: 0
机构:
Chaim Sheba Med Ctr, Pediat Neurol Unit, Ramat Gan, Israel
Chaim Sheba Med Ctr, Dept Diagnost Imaging, Ramat Gan, Israel Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel

Leshinsky-Silver, Esther
论文数: 0 引用数: 0
h-index: 0
机构:
Wolfson Med Ctr, Inst Med Genet, Holon, Israel
Wolfson Med Ctr, Pediat Neurol Unit, Holon, Israel Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel

Flusser, Hagit
论文数: 0 引用数: 0
h-index: 0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel

Sivan, Sara
论文数: 0 引用数: 0
h-index: 0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel

Soll, Dieter
论文数: 0 引用数: 0
h-index: 0
机构:
Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT USA
Yale Univ, Dept Chem, New Haven, CT USA Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel

Lerman-Sagie, Tally
论文数: 0 引用数: 0
h-index: 0
机构:
Wolfson Med Ctr, Inst Med Genet, Holon, Israel
Wolfson Med Ctr, Pediat Neurol Unit, Holon, Israel Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel

Birk, Ohad S.
论文数: 0 引用数: 0
h-index: 0
机构:
Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel
Soroka Univ, Med Ctr, Genet Inst, Beer Sheva, Israel Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel
[6]
Signal Recognition Particle: An Essential Protein-Targeting Machine
[J].
Akopian, David
;
Shen, Kuang
;
Zhang, Xin
;
Shan, Shu-ou
.
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 82,
2013, 82
:693-721

Akopian, David
论文数: 0 引用数: 0
h-index: 0
机构:
CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA

Shen, Kuang
论文数: 0 引用数: 0
h-index: 0
机构:
CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA

Zhang, Xin
论文数: 0 引用数: 0
h-index: 0
机构:
CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA

Shan, Shu-ou
论文数: 0 引用数: 0
h-index: 0
机构:
CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
[7]
Germline BRCA1 mutations predispose to pancreatic adenocarcinoma
[J].
Al-Sukhni, Wigdan
;
Rothenmund, Heidi
;
Borgida, Ayelet Eppel
;
Zogopoulos, George
;
O'Shea, Anne-Marie
;
Pollett, Aaron
;
Gallinger, Steven
.
HUMAN GENETICS,
2008, 124 (03)
:271-278

Al-Sukhni, Wigdan
论文数: 0 引用数: 0
h-index: 0
机构:
Samuel Lunenfeld Res Inst, Gallinger Lab, Toronto, ON M5G 1X5, Canada
Univ Toronto, Div Gen Surg, Dept Surg, Toronto, ON, Canada Samuel Lunenfeld Res Inst, Gallinger Lab, Toronto, ON M5G 1X5, Canada

Rothenmund, Heidi
论文数: 0 引用数: 0
h-index: 0
机构:
Samuel Lunenfeld Res Inst, Gallinger Lab, Toronto, ON M5G 1X5, Canada Samuel Lunenfeld Res Inst, Gallinger Lab, Toronto, ON M5G 1X5, Canada

Borgida, Ayelet Eppel
论文数: 0 引用数: 0
h-index: 0
机构:
Samuel Lunenfeld Res Inst, Gallinger Lab, Toronto, ON M5G 1X5, Canada Samuel Lunenfeld Res Inst, Gallinger Lab, Toronto, ON M5G 1X5, Canada

论文数: 引用数:
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O'Shea, Anne-Marie
论文数: 0 引用数: 0
h-index: 0
机构:
Samuel Lunenfeld Res Inst, Gallinger Lab, Toronto, ON M5G 1X5, Canada Samuel Lunenfeld Res Inst, Gallinger Lab, Toronto, ON M5G 1X5, Canada

Pollett, Aaron
论文数: 0 引用数: 0
h-index: 0
机构:
Samuel Lunenfeld Res Inst, Gallinger Lab, Toronto, ON M5G 1X5, Canada Samuel Lunenfeld Res Inst, Gallinger Lab, Toronto, ON M5G 1X5, Canada

Gallinger, Steven
论文数: 0 引用数: 0
h-index: 0
机构:
Samuel Lunenfeld Res Inst, Gallinger Lab, Toronto, ON M5G 1X5, Canada
Univ Toronto, Div Gen Surg, Dept Surg, Toronto, ON, Canada Samuel Lunenfeld Res Inst, Gallinger Lab, Toronto, ON M5G 1X5, Canada
[8]
Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus
[J].
Alazami, Anas M.
;
Hijazi, Hadia
;
Al-Dosari, Mohammed S.
;
Shaheen, Ranad
;
Hashem, Amal
;
Aldahmesh, Mohammed A.
;
Mohamed, Jawahir Y.
;
Kentab, Amal
;
Salih, Mustafa A.
;
Awaji, Ali
;
Masoodi, Tariq A.
;
Alkuraya, Fowzan S.
.
JOURNAL OF MEDICAL GENETICS,
2013, 50 (07)
:425-430

Alazami, Anas M.
论文数: 0 引用数: 0
h-index: 0
机构:
King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia

Hijazi, Hadia
论文数: 0 引用数: 0
h-index: 0
机构:
King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia

Al-Dosari, Mohammed S.
论文数: 0 引用数: 0
h-index: 0
机构:
King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia
King Saud Univ, Coll Pharm, Dept Pharmacognosy, Riyadh, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia

Shaheen, Ranad
论文数: 0 引用数: 0
h-index: 0
机构:
King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia

Hashem, Amal
论文数: 0 引用数: 0
h-index: 0
机构: King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia

Aldahmesh, Mohammed A.
论文数: 0 引用数: 0
h-index: 0
机构:
King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia

Mohamed, Jawahir Y.
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King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia

Kentab, Amal
论文数: 0 引用数: 0
h-index: 0
机构:
Prince Sultan Mil & Med City, Dept Pediat, Riyadh, Saudi Arabia
King Khalid Univ Hosp, Dept Pediat, Riyadh 11472, Saudi Arabia
King Saud Univ, Coll Med, Riyadh 11461, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia

Salih, Mustafa A.
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h-index: 0
机构:
King Khalid Univ Hosp, Dept Pediat, Riyadh 11472, Saudi Arabia
King Saud Univ, Coll Med, Riyadh 11461, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia

Awaji, Ali
论文数: 0 引用数: 0
h-index: 0
机构:
Jaizan Cent Hosp, Dept Pediat, Jaizan, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia

Masoodi, Tariq A.
论文数: 0 引用数: 0
h-index: 0
机构: King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia

Alkuraya, Fowzan S.
论文数: 0 引用数: 0
h-index: 0
机构:
King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia
King Khalid Univ Hosp, Dept Pediat, Riyadh 11472, Saudi Arabia
King Saud Univ, Coll Med, Riyadh 11461, Saudi Arabia
King Faisal Specialist Hosp & Res Ctr, Human Canc Genom Res, Riyadh 11211, Saudi Arabia
Alfaisal Univ, Coll Med, Dept Anat & Cell Biol, Riyadh, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia
[9]
Loss of Function Mutation in LARP7, Chaperone of 7SK ncRNA, Causes a Syndrome of Facial Dysmorphism, Intellectual Disability, and Primordial Dwarfism
[J].
Alazami, Anas M.
;
Al-Owain, Mohammad
;
Alzahrani, Fatema
;
Shuaib, Taghreed
;
Al-Shamrani, Hussain
;
Al-Falki, Yahya H.
;
Al-Qahtani, Saleh M.
;
Alsheddi, Tarfa
;
Colak, Dilek
;
Alkuraya, Fowzan S.
.
HUMAN MUTATION,
2012, 33 (10)
:1429-1434

Alazami, Anas M.
论文数: 0 引用数: 0
h-index: 0
机构: King Faisal Specialist Hosp & Res Ctr, Dev Genet Unit, Dept Genet, Riyadh 11211, Saudi Arabia

Al-Owain, Mohammad
论文数: 0 引用数: 0
h-index: 0
机构:
King Faisal Specialist Hosp & Res Ctr, Dept Med Genet, Riyadh 11211, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dev Genet Unit, Dept Genet, Riyadh 11211, Saudi Arabia

Alzahrani, Fatema
论文数: 0 引用数: 0
h-index: 0
机构: King Faisal Specialist Hosp & Res Ctr, Dev Genet Unit, Dept Genet, Riyadh 11211, Saudi Arabia

Shuaib, Taghreed
论文数: 0 引用数: 0
h-index: 0
机构: King Faisal Specialist Hosp & Res Ctr, Dev Genet Unit, Dept Genet, Riyadh 11211, Saudi Arabia

Al-Shamrani, Hussain
论文数: 0 引用数: 0
h-index: 0
机构:
King Faisal Specialist Hosp & Res Ctr, Dept Pediat, Riyadh 11211, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dev Genet Unit, Dept Genet, Riyadh 11211, Saudi Arabia

Al-Falki, Yahya H.
论文数: 0 引用数: 0
h-index: 0
机构:
King Khalid Univ, Dept Surg, Div Ophthalmol, Abha, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dev Genet Unit, Dept Genet, Riyadh 11211, Saudi Arabia

Al-Qahtani, Saleh M.
论文数: 0 引用数: 0
h-index: 0
机构:
King Khalid Univ, Dept Pediat, Abha, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dev Genet Unit, Dept Genet, Riyadh 11211, Saudi Arabia

Alsheddi, Tarfa
论文数: 0 引用数: 0
h-index: 0
机构: King Faisal Specialist Hosp & Res Ctr, Dev Genet Unit, Dept Genet, Riyadh 11211, Saudi Arabia

Colak, Dilek
论文数: 0 引用数: 0
h-index: 0
机构:
King Faisal Specialist Hosp & Res Ctr, Dept Biostat Epidemiol & Sci Comp, Riyadh 11211, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dev Genet Unit, Dept Genet, Riyadh 11211, Saudi Arabia

Alkuraya, Fowzan S.
论文数: 0 引用数: 0
h-index: 0
机构:
King Faisal Specialist Hosp & Res Ctr, Dev Genet Unit, Dept Genet, Riyadh 11211, Saudi Arabia
Alfaisal Univ, Coll Med, Dept Anat & Cell Biol, Riyadh, Saudi Arabia
King Saud Univ, Dept Pediat, King Khalid Univ Hosp, Riyadh, Saudi Arabia
King Saud Univ, Coll Med, Riyadh 11461, Saudi Arabia King Faisal Specialist Hosp & Res Ctr, Dev Genet Unit, Dept Genet, Riyadh 11211, Saudi Arabia
[10]
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
[J].
Amir, RE
;
Van den Veyver, IB
;
Wan, M
;
Tran, CQ
;
Francke, U
;
Zoghbi, HY
.
NATURE GENETICS,
1999, 23 (02)
:185-188

Amir, RE
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA

Van den Veyver, IB
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA

Wan, M
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA

Tran, CQ
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA

Francke, U
论文数: 0 引用数: 0
h-index: 0
机构: Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA

Zoghbi, HY
论文数: 0 引用数: 0
h-index: 0
机构:
Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA