Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation.

  F Giraudeau AuthorId : 1171219
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  L Taine AuthorId : 1171220
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  V Biancalana ¹ AuthorId : 1171221
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  B Delobel ² AuthorId : 1171222
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  H Journel AuthorId : 1171223
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  C Missirian ³ AuthorId : 1089164
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  D Lacombe ⁴ AuthorId : 1171224
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  D Bonneau ^{5, 6} AuthorId : 1171225
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  P Parent ⁷ AuthorId : 1171226
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  D Aubert ⁸ AuthorId : 903273
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  Y Hauck ⁹ AuthorId : 1171227
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  M F Croquette ¹⁰ AuthorId : 1171228
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  A Toutain ¹¹ AuthorId : 1171229
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  M G Mattei ¹² AuthorId : 1171230
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  H A Loiseau ¹³ AuthorId : 1171231
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  A David ¹⁴ AuthorId : 934380
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  Gilles Vergnaud ^{15, 9} AuthorId : 231027

Author IdHAL : gilles-vergnaud ResearcherId : http://www.researcherid.com/rid/P-1304-2015 ORCID : https://orcid.org/0000-0003-0913-194X