MMG PUBLICATIONS

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Results: 4196  publications found.

Popp B, .  et al. 0

Tamer C

Hellenbroich Y
Villard L - issue: von Spiczak S - volume: T - pages: Rauch A.


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Carlos, .  et al. 0

Christa Lese; Weiss

Richard J.; Dobyns
- issue: and is known as ""bilateral perisylvian polymicrogyria"" (BPP). Most cases are sporadic - volume: although several families have been observed with multiple affected members - pages: and maximal.


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Genomics. 1997 Jul 15, .  et al. 0

Villard L

10.1006/geno.1997.4793
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, .  et al. 0

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Vera M., .  et al. 0

Marlène; Doco-Fenzy

Pierre; Moutton
- issue: Juliette; Man - volume: Heng-Ye";Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth;Human Molecular Genetics;;1460-2083;10.1093/hmg/ddt187;;Existence of a discrete new X-linked intellectual d - pages: Céline; Villard.


Chantal, .  et al. 0

Josette; Villard

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Florent, .  et al. 0

Scott J.; Hongjie

Sukhan; Allen
Grazia Maria Simonetta; Hehr - issue: Elise; de Wit - volume: Marie C. Y.; Wilke - pages: Jacqueline; Villard.


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Am J Hum Genet. 1997 Jul, .  et al. 0

Ronce N

10.1016/S0002-9297(07)64297-9
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Louboutin JP, .  et al. 0

Recan D

Fontes M. "Eur J Hum Genet. 2000 Feb;8(2):125-9. doi: 10.1038/sj.ejhg.5200432." Villard L Eur J...
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indicated moderate-to-severe ID with autistic features, .  et al. 0

strabismus in all patients

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, .  et al. 0

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epilepsy, .  et al. 0

diffuse dysgyria

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, .  et al. 0

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Somat Cell Mol Genet. 1997 Mar, .  et al. 0

Villard L

10.1007/BF02679972
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H, .  et al. 0

Bastaraud SC

Forsythe E
Kamien B - issue: Levy J - volume: Guet A - pages: de Villemeur TB.


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