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  1. Cohesin and human disease. (0 replies)
  2. Cornelia de lange syndrome (0 replies)
  3. Prevalence of autism spectrum phenomenology in cornelia de lange and cri du chat syndromes. (0 replies)
  4. Deletion of 8p23.1 with features of cornelia de lange syndrome and congenital diaphragmatic hernia and a review of deletions of 8p23.1 to 8pter ? a further locus for cornelia de lange syndrome (0 replies)
  5. Health and sleep problems in cornelia de lange syndrome: a case control study (0 replies)
  6. [head & neck] temporal bone ct findings in cornelia de lange syndrome (0 replies)
  7. Temporal bone ct findings in cornelia de lange syndrome. (0 replies)
  8. Cornelia de lange syndrome (0 replies)
  9. Facial expression of affect in children with cornelia de lange syndrome (0 replies)
  10. Genomic organisation of the human chordin gene and mutation screening of candidate cornelia de lange syndrome genes (0 replies)
  11. Functional links between
    drosophila
    nipped-b and cohesin in somatic and meiotic cells     (0 replies)
  12. The behavioural phenotype of cornelia de lange syndrome: a study of 56 individuals (0 replies)
  13. Cecal volvulus in children with mental disability (0 replies)
  14. Clinical score of 62 italian patients with cornelia de lange syndrome and correlations with the presence and type of nipbl mutation (0 replies)
  15. Syndromes and disorders associated with omphalocele (iii): single gene disorders, neural tube defects, diaphragmatic defects and others. (0 replies)
  16. Cornelia de lange syndrome: clinical review, diagnostic and scoring systems, and anticipatory guidance (0 replies)
  17. Scientific abstract submissions presented at the second national scientific symposium in conjunction with the cornelia de lange syndrome foundation 25th national meeting june 22, 2006 (0 replies)
  18. Single gene disorders associated with congenital diaphragmatic hernia (0 replies)
  19. Prenatal/neonatal pathology in two cases of cornelia de lange syndrome harboring novel mutations of nipbl. (0 replies)
  20. Large genomic rearrangements in nipbl are infrequent in cornelia de lange syndrome (0 replies)
  21. A case of cornelia de lange syndrome from sudan (0 replies)
  22. Sponsorship Opportunity (0 replies)
  23. Mutations in cohesin complex members smc3 and smc1a cause a mild variant of cornelia de lange syndrome with predominant mental retardation (0 replies)
  24. Comprehensive mutational analysis of a cohort of swedish cornelia de lange syndrome patients (0 replies)
  25. Comprehensive mutational analysis of a cohort of swedish cornelia de lange syndrome patients (0 replies)
  26. See your message here (0 replies)
  27. Paternal gonadal mosaicism of nipbl mutation in a father of siblings with cornelia de lange syndrome (0 replies)
  28. Paternal gonadal mosaicism of nipbl mutation in a father of siblings with cornelia de lange syndrome (0 replies)
  29. A malay boy with the cornelia de lange syndrome: clinical and molecular findings. (0 replies)
  30. A malay boy with the cornelia de lange syndrome: clinical and molecular findings. (0 replies)
  31. [original articles] genotype-phenotype correlations of 39 patients with cornelia de lange syndrome: the dutch experience (0 replies)
  32. [original articles] genotype-phenotype correlations of 39 patients with cornelia de lange ... (0 replies)
  33. Effects of social context on social interaction and self-injurious behavior in cornelia de lange syndrome. (0 replies)
  34. Anoxic-epileptic seizures in cornelia de lange syndrome: case report of epileptic seizures induced by obstructive apnea. (0 replies)
  35. Calcific bicuspid aortic valve disease in a patient with cornelia de lange syndrome: linking altered notch signaling to aortic valve disease. (0 replies)
  36. Ophthalmic molecular genetics: ophthalmologic findings in cornelia de lange syndrome: a genotype-phenotype correlation study (0 replies)
  37. Ophthalmic molecular genetics: ophthalmologic findings in cornelia de lange syndrome: a ... (0 replies)
  38. X-linked cornelia de lange syndrome owing to smc1l1 mutations (0 replies)
  39. X-linked cornelia de lange syndrome owing to smc1l1 mutations (0 replies)
  40. Otitis media with effusion and hearing loss in children with cornelia de lange syndrome (0 replies)
  41. Molecular glue with new effect (0 replies)
  42. 'molecular glue' cohesin acts as regulator of gene expression (0 replies)
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