(Q24306615)

English

A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib

scientific article

Statements

A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib (English)
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Nicolas Richard
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Genevieve Abeguilé
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Nadia Coudray
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Hervé Mittre
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Nicolas Gruchy
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Pascal Cathebras
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May 2012
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97
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5
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E863-7
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Identifiers

 
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