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1. A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall-Smith Syndrome.

4. Large-scale open-source three-dimensional growth curves for clinical facial assessment and objective description of facial dysmorphism.

7. Consensus recommendations on organization of care for individuals with Phelan-McDermid syndrome

9. Identification of cellular retinoic acid binding protein 2 (CRABP2) as downstream target of nuclear factor 1/X (NFIX): implications for skeletal dysplasia syndromes

10. Diagnosis and management in Rubinstein-Taybi syndrome: first international consensus statement

12. Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study

15. No Pathogenic DICER1 Gene Variants in a Cohort Study of 28 Children With Congenital Pulmonary Airway Malformation

16. Diagnosis and management in Rubinstein-Taybi syndrome: first international consensus statement

17. Diagnosis and management in Rubinstein-Taybi syndrome:first international consensus statement

18. Diagnosis and management in Rubinstein-Taybi syndrome: first international consensus statement

19. Identification of cellular retinoic acid binding protein 2 (CRABP2) as downstream target of nuclear factor I/X (NFIX): implications for skeletal dysplasia syndromes.

20. Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1

24. DOORS syndrome and a recurrent truncating ATP6V1B2 variant

25. De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay

26. List of Contributors

28. Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.

29. No Pathogenic DICER1 Gene Variants in a Cohort Study of 28 Children With Congenital Pulmonary Airway Malformation

30. Self-injurious behavior

31. Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations

32. Mapping the human DC lineage through the integration of high-dimensional techniques

34. Identification of 34 novel and 56 known FOXL2 mutations in patients with blepharophimosis syndrome

36. European lipodystrophy registry: background and structure

37. Malan Syndrome

38. Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement

39. Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome

40. Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas

41. Definition and clinical variability of SHANK3-related Phelan-McDermid syndrome

42. Consensus recommendations on organization of care for individuals with Phelan-McDermid syndrome

43. A mouse model with a frameshift mutation in the nuclear factor I/X (NFIX) gene has phenotypic features of Marshall-Smith Syndrome

44. Clinical Disorders of Primary Malfunctioning of the Lymphatic System

47. A Pellino‐2 variant is associated with constitutive NLRP3 inflammasome activation in a family with ocular pterygium–digital keloid dysplasia

48. Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome

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