Search

Your search keyword '"St-Onge J"' showing total 193 results

Search Constraints

Start Over You searched for: Author "St-Onge J" Remove constraint Author: "St-Onge J"
193 results on '"St-Onge J"'

Search Results

5. Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management

9. Peripheral Oxidative Stress Markers Are Related To Vascular Risk Factors And Subcortical Small Vessel Disease

11. De novo missense mutations in the X-linked TFE3 gene cause intellectual disability with pigmentary mosaicism and storage disorder-like features

13. Nursing Perspective on the Confusion Assessment Method: a Qualitative Focus Group Study

14. P.048 Characterization of somatic mutations in mTOR pathway genes in focal cortical dysplasias

15. Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia

16. Caractérisation clinique et génétique d’une nouvelle dysplasie ectodermique en mosaïque

17. 616 Postzygotic mutations of RHOA cause a mosaic neuroectodermal syndrome

18. Autosomal recessive variations of TBX6 , from congenital scoliosis to spondylocostal dysostosis

19. Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes

20. De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome

21. Mutation en mosaïque de KITLG dans l’hypermélanose nævoïde

22. Mosaic‐activating FGFR2 mutation in two fetuses with papillomatous pedunculated sebaceous naevus

24. Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral–facial–digital syndrome with short stature and brachymesophalangia

25. Mutations activatrices de mTOR en mosaïque dans l’hypomélanose d’Ito avec mégalencéphalie

26. Mutations activatrices de GNA11 et GNAQ en mosaïque dans les phacomatoses pigmento-vasculaires et les taches mongoliques étendues

27. Clinical reappraisal of SHORT syndrome withPIK3R1mutations: toward recommendation for molecular testing and management

29. Usability evaluation of the progress note construction set

30. Shift in metabolic fuel in acylation-stimulating protein-deficient mice following a high-fat diet.

31. Mosaic-activating FGFR2 mutation in two fetuses with papillomatous pedunculated sebaceous naevus.

32. Medical education must make room for student-specific ethical dilemmas

43. Validation of a simple index (SIisOGTT) of insulin sensitivity in a population of sedentary men.

45. The stimulation-induced increase in skeletal muscle glycogen synthase content is impaired in carriers of the glycogen synthase XbaI gene polymorphism.

46. Runoff runs amok.

47. Mutations activatrices de GNA11 et GNAQen mosaïque dans les phacomatoses pigmento-vasculaires et les taches mongoliques étendues

49. Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes

50. The oral-facial-digital syndrome gene C2CD3 encodes a positive regulator of centriole elongation

Catalog

Books, media, physical & digital resources