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2. MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype

5. Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national survey

10. Fraser syndrome without cryptophthalmos: Two cases

14. MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations

15. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

17. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.

18. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

23. Phenotypic spectrum of STRA6 mutations: from matthew-wood syndrome to non-lethal anophthalmia.

25. Phacomatosis pigmentokeratotica associated with hypophosphataemic rickets, pheochromocytoma and multiple basal cell carcinomas

26. Nager syndrome: confirmation ofSF3B4haploinsufficiency as the major cause

27. Split hand/foot malformation with long-bone deficiency andBHLHA9duplication: report of 13 new families

28. Malformaciones congénitas de los miembros: de la clasificación al diagnóstico

29. Clasificación de las malformaciones congénitas de los miembros

30. What can we learn from old microdeletion syndromes using array-CGH screening?

33. MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations

34. Société Française d’Orthopédie Pédiatrique

39. Prenatal diagnosis of metatropic dwarfism

42. Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome

45. The GAPO syndrome

48. Functional characterization vs in silico prediction for TBX5 missense and splice variants in Holt-Oram syndrome.

49. Executive functioning in adolescents and adults with Silver-Russell syndrome.

50. TRIT1 deficiency: Two novel patients with four novel variants.

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