(Q34957544)
Statements
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Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype (English)
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T Kleefstra
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W A van Zelst-Stams
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W M Nillesen
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V Cormier-Daire
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G Houge
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N Foulds
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M van Dooren
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M H Willemsen
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R Pfundt
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A Turner
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M Wilson
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A Rauch
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M Zenker
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M P Adam
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C Davies
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A González-Meneses López
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R Casalone
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A Weber
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L A Brueton
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A Delicado Navarro
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M Palomares Bralo
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S P A Stegmann
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H G Yntema
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H van Bokhoven
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H G Brunner
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Identifiers
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