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7. De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

8. De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

9. Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator

10. Identification of Intellectual Disability Genes in Female Patients with a Skewed X-Inactivation Pattern

11. Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator

12. Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems

22. Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder

24. Partial monosomy 11q and trisomy 12q: variable expression in two siblings

25. De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

26. Recurrent De Novo Mutations in PACS1 Cause Defective Cranial-Neural-Crest Migration and Define a Recognizable Intellectual-Disability Syndrome

27. Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1

28. Triplication of distal chromosome 10q

29. Partial DiGeorge syndrome in two patients with a 10p rearrangement

31. Increased levels of low-density lipoprotein oxidation in patients with familial hypercholesterolemia and in end-stage renal disease patients on hemodialysis.

35. Cri du chat syndrome: Changing phenotype in older patients

44. Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3–p22.2 (MRX49) and Xp11.3–p11.21 (MRX50)

47. Benthic studies of the Southern Bight of the North Sea and its adjacent continental estuaries: Progress Report 1

50. Art. 15. Prosecutor

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