L. Villard And NotSyndrome complexe

List of bibliographic references

Number of relevant bibliographic references: 3.

Ident.	Authors (with country if any)	Title
002941	C. Cardoso [France] ; A. Boys [Australie] ; E. Parrini [Italie] ; C. Mignon-Ravix [France] ; J. M. Mcmahon [Australie] ; S. Khantane [France] ; E. Bertini [Italie] ; E. Pallesi [France] ; C. Missirian [France] ; O. Zuffardi [Italie] ; F. Novara [Italie] ; L. Villard [France] ; S. Giglio [Italie] ; B. Chabrol [France] ; H. R. Slater [Australie] ; A. Moncla [France] ; I. E. Scheffer [Australie] ; R. Guerrini [Italie]	Periventricular heterotopia, mental retardation, and epilepsy associated with 5ql4.3-ql5 deletion
004B88	V. Cantagrel [France] ; A.-M. Lossi [France] ; S. Boulanger [Belgique] ; D. Depetris [France] ; M.-G. Mattei [France] ; J. Gecz [Australie] ; C. E. Schwartz [États-Unis] ; L. Van Maldergem [Belgique] ; L. Villard [France]	Disruption of a new X linked gene highly expressed in brain in a family with two mentally retarded males
005E40	L. Villard [France] ; S. Briault [France] ; A.-M. Lossi [France] ; C. Paringaux [France] ; J. Belougne [France] ; L. Colleaux [France] ; D. R. Pincus [Australie] ; E. Woollatt [Australie] ; J. Lespinasse [France] ; A. Munnich [France] ; C. Moraine [France] ; M. Fontes [France] ; J. Gecz [Australie]	Two unrelated patients with inversions of the X chromosome and non-specific mental retardation : physical and transcriptional mapping of their common breakpoint region in Xq13.1

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