cytosine has been researched along with Auditory Processing Disorder, Central in 2 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Myotonic dystrophy is considered a true dominant condition with no difference in the phenotype between heterozygous and homozygous cases." | 1.35 | Homozygous myotonic dystrophy with craniosynostosis. ( Cerghet, M; Mahbubul Huq, AH; Serajee, FJ; Tapos, D, 2008) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Renda, MM | 1 |
| Voigt, RG | 1 |
| Babovic-Vuksanovic, D | 1 |
| Highsmith, WE | 1 |
| Vinson, SS | 1 |
| Sadowski, CM | 1 |
| Hagerman, RJ | 1 |
| Cerghet, M | 1 |
| Tapos, D | 1 |
| Serajee, FJ | 1 |
| Mahbubul Huq, AH | 1 |
2 other studies available for cytosine and Auditory Processing Disorder, Central
| Article | Year |
|---|---|
Neurodevelopmental disabilities in children with intermediate and premutation range fragile X cytosine-guanine-guanine expansions.
Topics: Adolescent; Attention Deficit Disorder with Hyperactivity; Child; Child Development Disorders, Perva | 2014 |
Homozygous myotonic dystrophy with craniosynostosis.
Topics: Alleles; Brain; Child, Preschool; Cranial Sutures; Craniosynostoses; Cytosine; DNA Mutational Analys | 2008 |