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Archives of Ophthalmology
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Archives of Ophthalmology
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Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy
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Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy
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Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy
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A novel founder BBS1 mutation explains a unique high prevalence of Bardet-Biedl...
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A novel founder BBS1 mutation explains a unique high prevalence of Bardet-Biedl...
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A novel founder BBS1 mutation explains a unique high prevalence of Bardet-Biedl...
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3
Article in Journal/Newspaper
2
Author
Batbayli, Mustafa
2
Brøndum-Nielsen, Karen
2
Duno, Morten
2
Grønskov, Karen
2
Hjortshøj, Tina Duelund
2
Ostergaard, Elsebet
2
Rosenberg, Thomas
2
Vilhelmsen, Kaj
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Brøndum-Nielsen, K
1
Grønskov, K
1
Hjortshøj, T Duelund
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Rosenberg, T
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Clinical genetics
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Ophthalmology
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Laboratory Science
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HighWire Press (Stanford University)
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Archive ouverte HAL (Hyper Article en Ligne, CCSD - Centre pour la Communication Scientifique Directe)
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The University of Dublin, Trinity College: TARA (Trinity's Access to Research Archive)
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Université de Nantes: HAL-UNIV-NANTES
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Faroe Islands
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