MMG PUBLICATIONS

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Results: 4168  publications found.

cancer genetic predisposition (CGP) and cancers. PFMG2025 has addressed numerous challenges to set up an operational organizational framework. As of December the 31st 2023, .  et al. 0

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Villard L, .  et al. 0

Mancini J

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C.; Guerrini

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empowering patients and practitioners, .  et al. 0

and fostering collaborations with European partners. FUNDING: As of December the 31st 2023

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M., .  et al. 0

S.; Grezel

13 (40%)
- issue: 12 - volume: with Salmonella Muenchen the most common. Th - pages: Ferruch and a non-motile O:4.

Rooryck C, .  et al. 0

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Marchal C
Philip N - issue: Michel V - volume: Routon MC - pages: Boulay C.

Iu B., .  et al. 0

M. L.; Demidova

P. V.";[Genotype-phenotype correlations in Rett syndrome: the study of Russian cohort of patients];Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova / Ministerstvo Zdravookhraneniia I...
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N. J., .  et al. 0

L.; Fontés

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L., .  et al. 0

L.; Arnason

M.; George
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D., .  et al. 0

W. T.; Chiurazzi

E. C.; Kooy
1997.;American journal of medical genetics;;0148-7299;"10.1002/(sici)1096-8628(19990402)83:4<221::aid-ajmg1>3.0.co;2-k";;;02/04/1999;04/08/2025 08:04;04/08/2025 08:04;;221-236;;4;83;;Am J Med Genet;;;;;;;;eng;;;;;;;Place: United States PMID: 10208154 - issue: L.; Willems - volume: P. J.";Eighth International workshop on the fragile X syndrome and X-linked mental retardation - pages: C.; Tranebjaerg.

nausea, .  et al. 0

headache

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Mignon-Ravix C, .  et al. 0

Cacciagli P

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Kit, .  et al. 0

Deborah; Marçano

Philip; Lindsay
- issue: - volume: - pages: where unique mutations were found in the T-box-containing transcription factor TBX22. Here we report two new familial cases with novel missense and insertion mutations.

and can thus be applied to a large number of patients at a low cost in any given laboratory., .  et al. 0

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