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104 results on '"Manouvrier‐Hanu, S."'

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

8. Fraser syndrome without cryptophthalmos: Two cases

11. 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

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

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

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

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

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

22. Nager syndrome: confirmation ofSF3B4haploinsufficiency as the major cause

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

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

26. 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

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

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

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

32. Monoallelic and biallelic variants in LEF1 are associated with a new syndrome combining ectodermal dysplasia and limb malformations caused by altered WNT signaling.

33. Quality of life and mental health of adolescents and adults with Silver-Russell syndrome.

34. Performance of meta-predictors for the classification of MED13L missense variations, implication of raw parameters.

35. Identification of limb-specific Lmx1b auto-regulatory modules with Nail-patella syndrome pathogenicity.

36. Smith-Magenis syndrome: Clinical and behavioral characteristics in a large retrospective cohort.

37. Phenotypic spectrum of SHANK2-related neurodevelopmental disorder.

38. Confirmation of risk of cancer in blepharocheilodontic syndrome.

39. Mayer-Rokitansky-Künster-Hauser syndrome due to 2q12.1q14.1 deletion: PAX8 the causing gene?

40. Comprehensive In Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer Variants.

41. Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder.

42. Duplication of 10q24 locus: broadening the clinical and radiological spectrum.

43. Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variants.

44. Blepharocheilodontic syndrome is a CDH1 pathway-related disorder due to mutations in CDH1 and CTNND1.

45. Cerebellar hypoplasia with endosteal sclerosis is a POLR3-related disorder.

46. 9q33.3q34.11 microdeletion: new contiguous gene syndrome encompassing STXBP1, LMX1B and ENG genes assessed using reverse phenotyping.

47. Nail-Patella Syndrome: clinical and molecular data in 55 families raising the hypothesis of a genetic heterogeneity.

48. The disruption of a novel limb cis-regulatory element of SHH is associated with autosomal dominant preaxial polydactyly-hypertrichosis.

49. 15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients.

50. Myhre and LAPS syndromes: clinical and molecular review of 32 patients.

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