120 results on '"Holvoet M"'
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2. Samenwerkplaatsten, samen bouwen aan de toekomst van de wijk.: Urban Living Lab Breda (ULLB) exploreert nieuwe wegen in stedelijke samenwerking
3. ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarism
4. Idiopathic multicentric osteolysis presents early and is not linked to chromosome 18q21.1
5. EP-1691 IORT and stray radiation: comparison of 2 commercial linacs
6. Severe mental retardation - distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a 10q25 → qter deletion
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
13. Etiologisch-diagnostisch onderzoek bij 66 volwassen personen met mentale handicap verblijvend in een bezigheidstehuis
14. Rome Statute of the International Criminal Court. Art. 68: Protection of the victims and witnesses and their participation in the proceedings (§ 1.2-2)
15. Rule 94 ICTY RPE: Judicial notice before the ad hoc Tribunals
16. Rome Statute of the International Criminal Court. Art. 9: Elements of Crimes
17. Resolution 995, 8 November 1994 - International Criminal Tribunal for Rwanda, statute: Art. 20. Rights of the Accused
18. Resolution 995, 8 November 1994 - International Criminal Tribunal for Rwanda, statute. Art. 7: Territorial and temporal jurisdiction
19. Resolution 995, 8 November 1994 - International Criminal Tribunal for Rwanda, statute. Art. 14: Rules of procedure and evidence
20. Rome Statute of the International Criminal Court. Art. 51: Rules of procedure and evidence
21. International criminal law as global gaw: An assessment of the hybrid tribunals
22. Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder
23. Harmonizing Exclusion under the Refugee Convention by Reference to the Evidentiary Standards of International Criminal Law
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
30. Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50)
31. Increased levels of low-density lipoprotein oxidation in patients with familial hypercholesterolemia and in end-stage renal disease patients on hemodialysis.
32. A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation
33. Severe mental retardation - distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a lOq25→qter deletion
34. Physical map of a 1.5Mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint
35. Cri du chat syndrome: Changing phenotype in older patients
36. ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarism
37. Physical map of a 1.5 Mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint
38. Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: Unusual chromosome 9 variant
39. Cri du chat syndrome: Changing phenotype in older patients
40. Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.
41. Severe mental retardation - distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a lOq25→qter deletion.
42. A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation.
43. Cryptic translocation t(5;18) in familial mental retardation
44. Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3p22.2 (MRX49) and Xp11.3p11.21 (MRX50)
45. Benthic studies of the Southern Bight of the North Sea and its adjacent continental estuaries. Progress report 2. Fluctuation of the meiobenthic communities in the Westerschelde estuary
46. Benthic studies of the Southern Bight of the North Sea and its adjacent continental estuaries. Progress Report 1
47. Benthic studies of the Southern Bight of the North Sea and its adjacent continental estuaries: Progress Report 1
48. Idiopathic multicentric osteolysis presents early and is not linked to chromosome 18q21.1
49. Convergences and Divergences Between International Human Rights Law, International Criminal Law and International Humanitarian Law: Conclusions
50. Art. 15. Prosecutor
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