G. Morel
发表
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M. Kubota,
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European journal of medical genetics.
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients
L. Bouneau,
P. Calvas,
N. Chassaing,
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J. Pouget,
M. Soriani,
A. Chaussenot,
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Human mutation.
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M. Soriani,
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Annals of neurology.
E. Génin,
J. Pouget,
A. Chaussenot,
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A. Munnich,
S. Julia,
A. Toutain,
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Genetics in Medicine.
J. Melki,
A. Toutain,
A. Verloes,
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Orphanet Journal of Rare Diseases.
C. Rooryck,
L. Pasquier,
E. Colin,
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Frontiers in Genetics.
S. Banka,
L. Faivre,
C. Philippe,
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American Journal of Medical Genetics. Part A.
J. Alessandri,
M. Tallot,
P. Gueguen,
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J. Thevenon,
L. Faivre,
F. Escande,
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C. Depienne,
O. Guillin,
A. Afenjar,
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European journal of human genetics : EJHG.
C. Roy,
M. Ohana,
M. Jeung,
2018
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