thymine has been researched along with Auditory Processing Disorder, Central in 3 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 | 1 (33.33) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| van Kuilenburg, AB | 1 |
| Meijer, J | 1 |
| Dobritzsch, D | 1 |
| Meinsma, R | 1 |
| Duran, M | 1 |
| Lohkamp, B | 1 |
| Zoetekouw, L | 1 |
| Abeling, NG | 1 |
| van Tinteren, HL | 1 |
| Bosch, AM | 1 |
| Cerghet, M | 1 |
| Tapos, D | 1 |
| Serajee, FJ | 1 |
| Mahbubul Huq, AH | 1 |
| Henderson, MJ | 1 |
| Jones, S | 1 |
| Walker, P | 1 |
| Duley, J | 1 |
| Simmonds, HA | 1 |
3 other studies available for thymine and Auditory Processing Disorder, Central
| Article | Year |
|---|---|
Clinical, biochemical and genetic findings in two siblings with a dihydropyrimidinase deficiency.
Topics: Amidohydrolases; Amino Acid Sequence; Animals; Brain; Child, Preschool; Crystallography, X-Ray; Dict | 2007 |
Homozygous myotonic dystrophy with craniosynostosis.
Topics: Alleles; Brain; Child, Preschool; Cranial Sutures; Craniosynostoses; Cytosine; DNA Mutational Analys | 2008 |
Heterogeneity of symptomatology in two male siblings with thymine uraciluria.
Topics: Child, Preschool; Chromatography, High Pressure Liquid; Humans; Infant, Newborn; Language Developmen | 1995 |