共 154 条
[1]
Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality
[J].
Ackermann, Bastian
;
Kroeber, Sandra
;
Torres-Benito, Laura
;
Borgmann, Anke
;
Peters, Miriam
;
Barkooie, Seyyed Mohsen Hosseini
;
Tejero, Rocio
;
Jakubik, Miriam
;
Schreml, Julia
;
Milbradt, Janine
;
Wunderlich, Thomas F.
;
Riessland, Markus
;
Tabares, Lucia
;
Wirth, Brunhilde
.
HUMAN MOLECULAR GENETICS,
2013, 22 (07)
:1328-1347

Ackermann, Bastian
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany
Univ Cologne, Inst Genet, D-50931 Cologne, Germany
Univ Cologne, CMMC, D-50931 Cologne, Germany Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany

Kroeber, Sandra
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany
Univ Cologne, Inst Genet, D-50931 Cologne, Germany
Univ Cologne, CMMC, D-50931 Cologne, Germany Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany

Torres-Benito, Laura
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Seville, Fac Med, Dept Med Physiol & Biophys, Seville, Spain Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany

Borgmann, Anke
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cologne, Inst Zool, D-50931 Cologne, Germany Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany

Peters, Miriam
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany
Univ Cologne, Inst Genet, D-50931 Cologne, Germany
Univ Cologne, CMMC, D-50931 Cologne, Germany Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany

Barkooie, Seyyed Mohsen Hosseini
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany
Univ Cologne, Inst Genet, D-50931 Cologne, Germany
Univ Cologne, CMMC, D-50931 Cologne, Germany Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany

Tejero, Rocio
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Seville, Fac Med, Dept Med Physiol & Biophys, Seville, Spain Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany

Jakubik, Miriam
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany
Univ Cologne, Inst Genet, D-50931 Cologne, Germany
Univ Cologne, CMMC, D-50931 Cologne, Germany Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany

Schreml, Julia
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany
Univ Cologne, Inst Genet, D-50931 Cologne, Germany
Univ Cologne, CMMC, D-50931 Cologne, Germany Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany

Milbradt, Janine
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany
Univ Cologne, Inst Genet, D-50931 Cologne, Germany Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany

Wunderlich, Thomas F.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cologne, Inst Genet, D-50931 Cologne, Germany
Univ Cologne, CMMC, D-50931 Cologne, Germany
Univ Cologne, Cologne Excellence Cluster Cellular Stress Respon, D-50931 Cologne, Germany
Max Planck Inst Neurol Res, D-50931 Cologne, Germany Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany

论文数: 引用数:
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机构:

Tabares, Lucia
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Seville, Fac Med, Dept Med Physiol & Biophys, Seville, Spain Univ Cologne, Inst Human Genet, D-50931 Cologne, Germany

论文数: 引用数:
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机构:
[2]
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse
[J].
Akhmedov, NB
;
Piriev, NI
;
Chang, B
;
Rapoport, AL
;
Hawes, NL
;
Nishina, PM
;
Nusinowitz, S
;
Heckenlively, JR
;
Roderick, TH
;
Kozak, CA
;
Danciger, M
;
Davisson, MT
;
Farber, DB
.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
2000, 97 (10)
:5551-5556

Akhmedov, NB
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA

Piriev, NI
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA

Chang, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA

Rapoport, AL
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA

Hawes, NL
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA

Nishina, PM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA

Nusinowitz, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA

Heckenlively, JR
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA

Roderick, TH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA

Kozak, CA
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA

Danciger, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA

Davisson, MT
论文数: 0 引用数: 0
h-index: 0
机构: Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA

Farber, DB
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA
[3]
Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice
[J].
Anderson, Michael G.
;
Smith, Richard S.
;
Savinova, Olga V.
;
Hawes, Norman L.
;
Chang, Bo
;
Zabaleta, Adriana
;
Wilpan, Robert
;
Heckenlively, John R.
;
Davisson, Muriel
;
John, Simon W. M.
.
BMC GENETICS,
2001, 2 (1)

Anderson, Michael G.
论文数: 0 引用数: 0
h-index: 0
机构:
Howard Hughes Med Inst, Bar Harbor, ME USA
Jackson Lab, Bar Harbor, ME 04609 USA Howard Hughes Med Inst, Bar Harbor, ME USA

Smith, Richard S.
论文数: 0 引用数: 0
h-index: 0
机构:
Howard Hughes Med Inst, Bar Harbor, ME USA
Jackson Lab, Bar Harbor, ME 04609 USA Howard Hughes Med Inst, Bar Harbor, ME USA

Savinova, Olga V.
论文数: 0 引用数: 0
h-index: 0
机构:
Jackson Lab, Bar Harbor, ME 04609 USA Howard Hughes Med Inst, Bar Harbor, ME USA

Hawes, Norman L.
论文数: 0 引用数: 0
h-index: 0
机构:
Jackson Lab, Bar Harbor, ME 04609 USA Howard Hughes Med Inst, Bar Harbor, ME USA

Chang, Bo
论文数: 0 引用数: 0
h-index: 0
机构:
Jackson Lab, Bar Harbor, ME 04609 USA Howard Hughes Med Inst, Bar Harbor, ME USA

Zabaleta, Adriana
论文数: 0 引用数: 0
h-index: 0
机构:
Jackson Lab, Bar Harbor, ME 04609 USA Howard Hughes Med Inst, Bar Harbor, ME USA

Wilpan, Robert
论文数: 0 引用数: 0
h-index: 0
机构:
Jackson Lab, Bar Harbor, ME 04609 USA Howard Hughes Med Inst, Bar Harbor, ME USA

Heckenlively, John R.
论文数: 0 引用数: 0
h-index: 0
机构:
Jules Stein Eye Inst, Los Angeles, CA 90024 USA Howard Hughes Med Inst, Bar Harbor, ME USA

Davisson, Muriel
论文数: 0 引用数: 0
h-index: 0
机构:
Jackson Lab, Bar Harbor, ME 04609 USA Howard Hughes Med Inst, Bar Harbor, ME USA

John, Simon W. M.
论文数: 0 引用数: 0
h-index: 0
机构:
Howard Hughes Med Inst, Bar Harbor, ME USA
Jackson Lab, Bar Harbor, ME 04609 USA
Tufts Univ, Coll Med, Dept Ophthalmol, Boston, MA 02111 USA Howard Hughes Med Inst, Bar Harbor, ME USA
[4]
EXTENSIVE INTRAFAMILIAL AND INTERFAMILIAL PHENOTYPIC VARIATION AMONG PATIENTS WITH AUTOSOMAL-DOMINANT RETINAL DYSTROPHY AND MUTATIONS IN THE HUMAN RDS PERIPHERIN GENE
[J].
APFELSTEDTSYLLA, E
;
THEISCHEN, M
;
RUTHER, K
;
WEDEMANN, H
;
GAL, A
;
ZRENNER, E
.
BRITISH JOURNAL OF OPHTHALMOLOGY,
1995, 79 (01)
:28-34

APFELSTEDTSYLLA, E
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ESSEN GESAMTHSCH,HOSP EYE,D-45122 ESSEN,GERMANY

THEISCHEN, M
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ESSEN GESAMTHSCH,HOSP EYE,D-45122 ESSEN,GERMANY

RUTHER, K
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ESSEN GESAMTHSCH,HOSP EYE,D-45122 ESSEN,GERMANY

WEDEMANN, H
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ESSEN GESAMTHSCH,HOSP EYE,D-45122 ESSEN,GERMANY

GAL, A
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ESSEN GESAMTHSCH,HOSP EYE,D-45122 ESSEN,GERMANY

ZRENNER, E
论文数: 0 引用数: 0
h-index: 0
机构: UNIV ESSEN GESAMTHSCH,HOSP EYE,D-45122 ESSEN,GERMANY
[5]
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome
[J].
Arts, Heleen H.
;
Doherty, Dan
;
van Beersum, Sylvia E. C.
;
Parisi, Melissa A.
;
Letteboer, Stef J. F.
;
Gorden, Nicholas T.
;
Peters, Theo A.
;
Maerker, Tina
;
Voesenek, Krysta
;
Kartono, Aileen
;
Ozyurek, Hamit
;
Farin, Federico M.
;
Kroes, Hester Y.
;
Wolfrum, Uwe
;
Brunner, Han G.
;
Cremers, Frans P. M.
;
Glass, Ian A.
;
Knoers, Nine V. A. M.
;
Roepman, Ronald
.
NATURE GENETICS,
2007, 39 (07)
:882-888

Arts, Heleen H.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

论文数: 引用数:
h-index:
机构:

van Beersum, Sylvia E. C.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

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

Letteboer, Stef J. F.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Gorden, Nicholas T.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

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

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

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

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

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

Farin, Federico M.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

Kroes, Hester Y.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

论文数: 引用数:
h-index:
机构:

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

Cremers, Frans P. M.
论文数: 0 引用数: 0
h-index: 0
机构: Radboud Univ Nijmegen, Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands

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

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

Roepman, Ronald
论文数: 0 引用数: 0
h-index: 0
机构:
Radboud Univ Nijmegen, Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Ctr Mol Life Sci, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
[6]
CDH23 mutation and phenotype heterogeneity:: A profile of 107 diverse families with Usher syndrome and nonsyndromic deafness
[J].
Astuto, LM
;
Bork, JM
;
Weston, MD
;
Askew, JW
;
Fields, RR
;
Orten, DJ
;
Ohliger, SJ
;
Riazuddin, S
;
Morell, RJ
;
Khan, S
;
Riazuddin, S
;
Kremer, H
;
van Hauwe, P
;
Moller, CG
;
Cremers, CWRJ
;
Ayuso, C
;
Heckenlively, JR
;
Rohrschneider, K
;
Spandau, U
;
Greenberg, J
;
Ramesar, R
;
Reardon, W
;
Bitoun, P
;
Millan, J
;
Legge, R
;
Friedman, TB
;
Kimberling, WJ
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2002, 71 (02)
:262-275

Astuto, LM
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Bork, JM
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Weston, MD
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Askew, JW
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Fields, RR
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Orten, DJ
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Ohliger, SJ
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Riazuddin, S
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Morell, RJ
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Khan, S
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Riazuddin, S
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Kremer, H
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

van Hauwe, P
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Moller, CG
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Cremers, CWRJ
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Ayuso, C
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Heckenlively, JR
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Rohrschneider, K
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Spandau, U
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Greenberg, J
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Ramesar, R
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Reardon, W
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Bitoun, P
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Millan, J
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Legge, R
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Friedman, TB
论文数: 0 引用数: 0
h-index: 0
机构: Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA

Kimberling, WJ
论文数: 0 引用数: 0
h-index: 0
机构:
Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA Boys Town Natl Res Hosp, Ctr Study & Treatment Usher Syndrome, Omaha, NE 68131 USA
[7]
Pleiotropic effects of CEP290 (NPHP6) mutations extend to Meckel syndrome
[J].
Baala, Lekbir
;
Audollent, Sophie
;
Martinovic, Jelena
;
Ozilou, Catherine
;
Babron, Marie-Claude
;
Sivanandamoorthy, Sivanthiny
;
Saunier, Sophie
;
Salomon, Remi
;
Gonzales, Marie
;
Rattenberry, Eleanor
;
Esculpavit, Chantal
;
Toutain, Annick
;
Moraine, Claude
;
Parent, Philippe
;
Marcorelles, Pascale
;
Dauge, Marie-Christine
;
Roume, Joelle
;
Le Merrer, Martine
;
Meiner, Vardiella
;
Meir, Karen
;
Menez, Francoise
;
Beaufrere, Anne-Marie
;
Francannet, Christine
;
Tantau, Julia
;
Sinico, Martine
;
Dumez, Yves
;
MacDonald, Fiona
;
Munnich, Arnold
;
Lyonnet, Stanislas
;
Gubler, Marie-Claire
;
Genin, Emmanuelle
;
Johnson, Colin A.
;
Vekemans, Michel
;
Encha-Razavi, Ferechte
;
Attie-Bitach, Tania
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2007, 81 (01)
:170-179

Baala, Lekbir
论文数: 0 引用数: 0
h-index: 0
机构: Hop Necker Enfants Malad, Dept Genet, F-75743 Paris 15, France

Audollent, Sophie
论文数: 0 引用数: 0
h-index: 0
机构: Hop Necker Enfants Malad, Dept Genet, F-75743 Paris 15, France

Martinovic, Jelena
论文数: 0 引用数: 0
h-index: 0
机构: Hop Necker Enfants Malad, Dept Genet, F-75743 Paris 15, France

Ozilou, Catherine
论文数: 0 引用数: 0
h-index: 0
机构: Hop Necker Enfants Malad, Dept Genet, F-75743 Paris 15, France

Babron, Marie-Claude
论文数: 0 引用数: 0
h-index: 0
机构: Hop Necker Enfants Malad, Dept Genet, F-75743 Paris 15, France

Sivanandamoorthy, Sivanthiny
论文数: 0 引用数: 0
h-index: 0
机构: Hop Necker Enfants Malad, Dept Genet, F-75743 Paris 15, France

Saunier, Sophie
论文数: 0 引用数: 0
h-index: 0
机构: Hop Necker Enfants Malad, Dept Genet, F-75743 Paris 15, France

Salomon, Remi
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Gonzales, Marie
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Rattenberry, Eleanor
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Esculpavit, Chantal
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Toutain, Annick
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Moraine, Claude
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Parent, Philippe
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Marcorelles, Pascale
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Dauge, Marie-Christine
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Roume, Joelle
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Le Merrer, Martine
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Meiner, Vardiella
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Meir, Karen
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Menez, Francoise
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Beaufrere, Anne-Marie
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Francannet, Christine
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Tantau, Julia
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Sinico, Martine
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Dumez, Yves
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MacDonald, Fiona
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Munnich, Arnold
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Lyonnet, Stanislas
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Gubler, Marie-Claire
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Genin, Emmanuelle
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Johnson, Colin A.
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Vekemans, Michel
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Encha-Razavi, Ferechte
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Attie-Bitach, Tania
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