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Keyword [Intellectual disability]
Result: 1 - 20 | Page: 1 of 3
1. The Investigation And Analysis Of Oral Health Status And Behaviors Of Children And Adolescents With Intellectual Disability In Chendu
2. The Clinical And Genetic Etiology Study Of Infantile Spasms
3. A Critical Role Of RBM8a In Proliferation And Differentiation Of Embryonic Neural Progenitors
4. Group Work Intervention Study Of The Psychological Pressure Of Caregivers Of People With Intellectual Disabilities
5. X-linked Intellectual Disability Gene CUL4B Targets Jab1/CSN5for Degradation
6. Beijing Intellectually Disabled Children Aged0to6Referral Service Model Of Rehabilitation Research
7. Clinical And Cellular And Molecular Genetics Two Cases Of Chromosome Copy Number Abnormalities In Patients
8. Genome-wide Copy Number Variations Analysis In373Patients With Unexplained Intellectual Disability/Development Delay And Multiple Congenital Anomalities
9. Effect Of Audio-Visual Sensory Integration Training On Cognitive Ability Of Children With Intellectual Disabiiity
10. To Explore The Parental-of-origin Of De Novo And Pathogenic Copy Number Variation With Intellectual Disability And Other Congenital Birth Defects
11. Next-generation Sequencing And Molecular Analysis Of 3 Unexplained Intellectual Disability Patients
12. Genome-wide Copy Number Variations Analysis In 31 Patients With Unexplained Intellectual Disability/Developmental Delay
13. X-linked Intellectual Disability Gene CUL4B Inhibits The Self-renewal Of Neural Stem Cells Via Regulating Substrate Protein Prdx3
14. The Role Of Sorbs2 Gene In Dendritic Development,Synaptic Transmission And Cognitive Impairment
15. CRL4 Antagonizes SCFFbxo7-mediated Turnover Of Cereblon And BK Channel To Regulate Learning And Memory
16. Research On Prosocial Behavior Of Children With Intellectual Disability
17. Molecular Pathogenesis Of Renpenning Syndrome Caused By PQBP1 Mutations
18. Next-Generation Sequencing Identifies Pathogenesis And Diagnostic Strategy Of Intellectual Disability
19. The Investigation Of Genetic Etiology Of Unexplained Intellectual Disability/Global Developmental Delay
20. Loss Of Foxg1 Impairs The Development Of Cortical SST-Interneurons Leading To Abnormal Emotional And Social Behaviors
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