MMG PUBLICATIONS

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Results: 4167  publications found.

Florence, .  et al. 0

Gisèle; Michon

Alexandra; Mignot
Fabienne; Lesca - issue: Damien; Trauffler - volume: Adeline; Badens - pages: Estelle; De La Vaissière.

specific signals were easily detected for Mecp2_e1, .  et al. 0

whilst Mecp2_e2 was very difficult to detect by Western blot

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S., .  et al. 0

L.; Jolliet

which may have arisen due to inconsistencies in the geometrical approximation. System size effects are further explored by modifying the width of the strong gradient region at fixed system size....
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Epilepsia. 2011 Oct, .  et al. 0

Milh M

10.1111/j.1528-1167.2011.03181.x
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Walsh C, .  et al. 0

Novelli A

Capra V
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Saywell V, .  et al. 0

Burnet H

Moncla A
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and can present with early-onset epileptic encephalopathy without brain iron accumulation.European Journal of Human Genetics advance online publication, .  et al. 0

15 July 2015; doi:10.1038/ejhg.2015.159.";15/07/2015;07/03/2016 15:11;23/06/2020 08:43;;;;;;;Eur. J. Hum. Genet.;;;;;;;;ENG;;;;;PubMed;;PMID: 26173968

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, .  et al. 0

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BMC Neurosci. 2011 May 24, .  et al. 0

Panayotis N

10.1186/1471-2202-12-47
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Arnaud L, .  et al. 0

Barcia G

Leguern E
- issue: Weckhuysen S - volume: Keren B - pages: Valence S.

Ragusa A, .  et al. 0

Belougne J

Lacombe D
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Sandra, .  et al. 0

Pierre; Mignon-Ravix

Tony; Villard
indicate uniparental disomy or parental consanguinity that is suggestive of an increased probability of recessive disease. RESULTS: We screened 149 Lebanese probands with ID/ - issue: as well as regions of homozygosity - volume: that - pages: developmental delay (DD).

Nicolas, .  et al. 0

Ira; Dierssen

Jose I.; Balint
and aberrations in the distribution of this epigenetic mark may be involved in many neurological disorders - issue: Takao K.; Ferrer - volume: Isidre; Esteller - pages: Jean-Christophe; Avila.

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Am J Med Genet A. 2011 May, .  et al. 0

Mégarbané A

10.1002/ajmg.a.33938
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, .  et al. 0

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Chelly PJ, .  et al. 0

Tardieu PM

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a depressed nasal bridge, .  et al. 0

hypertelorism

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, .  et al. 0

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