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1,619 results on '"Centre for Medical Genetics"'

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1. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

2. Pregnancy termination at a viable stage in daily clinical practice

3. Peripheral precocious puberty in Li–Fraumeni syndrome: a case report and literature review of pure androgen-secreting adrenocortical tumors

4. Inhibition of PLK1 Destabilizes EGFR and Sensitizes EGFR-Mutated Lung Cancer Cells to Small Molecule Inhibitor Osimertinib

5. Twelve years of assessing the quality of preimplantation genetic testing for monogenic disorders

6. Further delineation of the KAT6B molecular and phenotypic spectrum

7. Clinical, cytogenetic and molecular characteristics of 14 T-ALL patients carrying the TCRβ-HOXA rearrangement: a study of the Groupe Francophone de Cytogénétique Hématologique

8. Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition

9. EDIR

10. Identification of differentially methylated regions in rare diseases from a single-patient perspective

11. The Basque Paradigm: Genetic Evidence of a Maternal Continuity in the Franco-Cantabrian Region since Pre-Neolithic Times

12. A systematic review and evidence assessment of monogenic gene-disease relationships in human female infertility and differences in sex development

13. ESHRE survey results and good practice recommendations on managing chromosomal mosaicism

14. Barriers and facilitators for the implementation of patient-centered care in cardiogenetics: a Delphi study among ERN GUARD-heart members

15. Arrhythmia and impaired myocardial function in heritable thoracic aortic disease: An international retrospective cohort study

16. Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorder

17. Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy

18. Blurring boundaries. Interviews with PGT couples about comprehensive chromosome screening

19. The Centriolar Adjunct–Appearance and Disassembly in Spermiogenesis and the Potential Impact on Fertility

22. ESHRE PGD Consortium data collection XIV-XV: cycles from January 2011 to December 2012 with pregnancy follow-up to October 2013

23. Growth and health outcome of 102 2-year-old children conceived after preimplantation genetic diagnosis or screening

24. Intergenerational Instability of the Expanded CTG Repeat in the DMPK Gene: Studies in Human Gametes and Preimplantation Embryos

25. Cognitive and psychomotor development of 5- to 6-year-old singletons born after PGD: a prospective case-controlled matched study

26. The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

27. Logics with Copy and Remove

28. Pyruvate dehydrogenase complex deficiency and absence of subunit X

29. Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations

30. (0) Save to: more options Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres

31. Human trophectoderm cells are not yet committed

32. Recruitment bias in chronic pain research

33. Long-term functioning following whiplash injury

34. Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias

35. Rapid, sensitive and discriminatory HbS and HbC mutation detection using High Resolution Melting Analysis

36. Preimplantation Genetic Diagnosis (PGD) for Cartilage Hair Hypopasia combined with Human Leukocyte Antigen (HLA)

37. METHYLATION OF THE CPG SITES IN THE MYOTONIC DYSTROPHY LOCUS DOES NOT CORRELATE WITH CTG EXPANSION SIZE OR WITH THE CONGENITAL FORM OF THE DISEASE

38. Developmental capacity and pregnancy rate of tetrahedral versus non-tetrahedral 4-cell stage human embryos

39. Molecular spectrum of androgen receptor gene alterations in Belgian patients

40. Mutation analysis of the NEMO gene in patients with Incontinentia Pigmenti

41. Neonatal outcome of children born after assisted reproduction with and without embryo biopsy. 38e Jaarlijkse Vergadering van de Belgische Vereniging voor Kindergeneeskunde. 19 en 20 maart 2010, Brussel

42. Pulse pressure and cardiovascular reactivity among ICSI conceived teenagers

43. Are children born after ICSI at risk for disturbed subcutaneous body fat accumulation and distribution at puberty?

44. Severe mitochondrial DNA depletion in infancy

45. Developmental regulation and decisions in the human preimplantation embryo

46. Oocyte donation is a risk factor for first trimester bleeding and pregnancy induced hypertension but without efffect on the perinatal outcome

47. Development and validation of a multiplex real-time PCR assay for simultaneous genotyping and human T-lymphotropic virus type 1, 2, and 3 proviral load determination

48. Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to the m.14487T>C mutation in ND6

49. Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24-32 mutation

50. The experience of two European preimplantation genetic diagnosis centres on human leukocyte antigen typing

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