MMG PUBLICATIONS

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Results: 4168  publications found.

, .  et al. 0

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Nat Genet. 1996 Apr, .  et al. 0

Villard L

10.1038/ng0496-359
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Philip N, .  et al. 0

Menten B

Grange DK
Bottani A - issue: Mortier G - volume: Friedman JM - pages: Gimelli S.


maturing neurons., .  et al. 0

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, .  et al. 0

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since 2018, .  et al. 0

with the French reference center for rare epilepsies (CRéER). RESULTS: Since 2014

SCN2A
- issue: account for one-sixth of patients and half of the diagnoses provided by the PAGEM. CONCLUSION: These results suggest that a gene-panel approach is an efficient first-tier test for the genetic diagnosis of Mendelian epileptic disorders. In a near futu - volume: French patients with ""drug-resistant epilepsies with seizure-onset in the first two-years of life"" can be - pages: SYNGAP1.


respectively. We postulate that a gene might be disrupted by one of the breakpoints., .  et al. 0

Inc.;;;;;;Place: United States PMID: 11078572

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Am J Hum Genet. 1996 Mar, .  et al. 0

Villard L

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F., .  et al. 0

A.; Labelle

J.; Anvret
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Eur J Hum Genet. 1996, .  et al. 0

Villard L

10.1159/000472225
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Girard N, .  et al. 0

Milh M

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Pierre, .  et al. 0

Eve; Legeai-Mallet

Laurent; Philip
- issue: there is evidence of generalized cartilage dysplasia - volume: - pages: and molecular data from two additional patients carrying balanced translocations involving the same 2q37.1 chromosome band and chromosomes 8 and 13.


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Cyril, .  et al. 0

Delphine; Bastaraud

Jane; Forsythe
Manoëlle; Kamien - issue: Anne Claude; Levy - volume: Jonathan; Guet - pages: Olga; de Villemeur.


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Mamm Genome. 1995 Sep, .  et al. 0

Villard L

10.1007/BF00352368
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