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American Society of Human Genetics - San Diego - October 18-22, 2014 Contact Search
 

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ASHG 2014 Abstract Submission Key Words

 

 

  1. amino acidemias
  2. assisted reproduction
  3. ataxia
  4. alternative splicing
  5. auditory system
  6. biochemical pathology
  7. biogenesis
  8. bioinformatics
  9. bone marrow transplantation
  10. bone/joint abnormalities
  11. brain/nervous system
  12. cancer
  13. cancer cytogenetics
  14. cancer syndromes
  15. candidate gene
  16. cardiovascular system
  17. cellular metabolism
  18. centromere structure/function
  19. channelopathies
  20. characterization of disorders
  21. characterization of syndromes
  22. chromatin immunoprecipitation
  23. chromosomal abnormalities
  24. chromosomal deletions
  25. chromosomal structure/function
  26. ciliopathies
  27. clinical applications of molecular cytogenetics
  28. clinical cytogenetics
  29. clinical history
  30. comparative mapping
  31. computational tools
  32. congenital anomaly
  33. contigs
  34. copy number/structural variation
  35. counseling
  36. CVD
  37. databases
  38. deformation
  39. delineation of diseases
  40. development
  41. diabetes
  42. diagnostics
  43. differentiation
  44. digital gene expression
  45. disruption
  46. dysmorphology
  47. education
  48. embryonic stem cells
  49. epidemiology
  50. endocrine system
  51. enzyme replacement therapy
  52. epilepsy
  53. expressed sequence tags
  54. ethical, legal and social issues
  55. etiology
  56. evolution
  57. evolutionary genetics
  58. expansion
  59. family history
  60. family linkage analysis
  61. fetal pathology
  62. fetal therapy
  63. FISH
  64. fragile X syndrome and FXTAS
  65. functional motifs
  66. gastrointestinal system
  67. gene environment interaction
  68. gene families
  69. gene localization
  70. gene therapy
  71. gene transfer methodologies
  72. genes in development
  73. genetic diversity
  74. genetic epidemiology
  75. genetic instability
  76. genetic mapping
  77. genetic testing
  78. genitourinary system
  79. genome scan
  80. genome sequencing
  81. genome-wide association
  82. genomic methodologies
  83. genomic structure
  84. genotype-phenotype correlations
  85. haplotype
  86. hematopoietic system
  87. identification of disease genes
  88. immune system
  89. imprinting
  90. infectious disease
  91. infertility
  92. inheritance modeling
  93. inheritance patterns
  94. limb
  95. linkage disequilibrium
  96. linkage mapping
  97. linkage methodology
  98. lymphatic system
  99. lysosomal diseases
  100. malformation
  101. mapping complex traits
  102. maps
  103. massively parallel sequencing
  104. maternal genetic disease
  105. maternal serum screening
  106. mathematical modeling
  107. intellectual and developmental disability
  108. metabolic disorder
  109. methodology
  110. methylation
  111. microarrays
  112. micro RNA
  113. mitochondria
  114. model organisms
  115. molecular pathophysiology
  116. morphogenesis
  117. muscular abnormalities
  118. mutation detection
  119. myotonic dystrophies
  120. natural history
  121. natural selection
  122. newborn screening
  123. neurodegeneration
  124. neurogenetics
  125. nervous system
  126. noncoding RNA
  127. oncogenesis
  128. organic acidurias
  129. pathogenesis
  130. peroxisomal diseases
  131. pharmacodynamics
  132. pharmacogenetics
  133. pharmacokinetics
  134. pharmacologic therapy
  135. phenotype
  136. physical mapping
  137. policy issues
  138. polyalanine disorders
  139. polyglutamine diseases
  140. polymorphism
  141. population genetics
  142. population structure
  143. preclinical trial
  144. predictive testing
  145. preimplantation diagnosis
  146. prenatal diagnosis
  147. proteomics
  148. psychosocial counseling issues
  149. psychosocial issues
  150. public health
  151. public, patient and professional education
  152. regulation of transcription
  153. reproductive genetics
  154. respiratory system
  155. risk assessment
  156. RNA
  157. RNAi
  158. RNA pathology
  159. skeletal system
  160. SNP analysis/discovery
  161. splicing mechanisms
  162. stem cell(s)
  163. structure/function
  164. susceptibility locus
  165. systems biology
  166. tandem mass spectroscopy
  167. telomere structure/function
  168. teratogens
  169. therapy
  170. transcription
  171. transcription factor
  172. transgenic model
  173. translational studies and preclinical trials
  174. transplantation
  175. transposable elements
  176. triplet and other repeats
  177. ultrasound diagnosis
  178. uniparental disomy
  179. visual systems
  180. viral vectors
  181. X-inactivation
  182. X-linked disease

 

 

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