PUBLICATIONS of MMG

Veuillez utiliser l'outil ci-dessous pour consulter nos publications par mots clés et/ou par équipe et/ou par année.

Suivez les liens pour consulter les publications sur le site de PubMed.



Rechercher une publication





Résultats : 4199  publications trouvées.

suggesting that it belongs to the clinical entity of rare congenital muscular dystrophies., .  et al. 0

- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .

Hum Mol Genet. 1998 Apr, .  et al. 0

Cardoso C

10.1093/hmg/7.4.679
- issue: - volume: - pages: .

Popp B, .  et al. 0

Tamer C

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

, .  et al. 0

- issue: - volume: - pages: .

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.

, .  et al. 0

- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .

Genomics. 1997 Jul 15, .  et al. 0

Villard L

10.1006/geno.1997.4793
- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .

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

- issue: - volume: - pages: .

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.

, .  et al. 0

- issue: - volume: - pages: .

Am J Hum Genet. 1997 Jul, .  et al. 0

Ronce N

10.1016/S0002-9297(07)64297-9
- issue: - volume: - pages: .

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...
- issue: - volume: - pages: .

indicated moderate-to-severe ID with autistic features, .  et al. 0

strabismus in all patients

- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .

epilepsy, .  et al. 0

diffuse dysgyria

- issue: - volume: - pages: .

, .  et al. 0

- issue: - volume: - pages: .