histidine has been researched along with Microcephaly in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Astudillo, MF; Bacino, CA; Burrage, LC; Chao, HT; Dai, H; Gibson, JB; Lalani, SR; Lee, BH; Lewis, RA; Lin, Y; Magyar, CL; Murdock, DR; Rosenfeld, JA; Tran, AA | 1 |
| Basel-Vanagaite, L; Dahary, D; Halevy, A; Har-Zahav, A; Haviv, A; Hellman-Aharony, S; Maya, I; Pasmanik-Chor, M; Shohat, M; Smirin-Yosef, P; Straussberg, R; Yeheskel, A | 1 |
1 review(s) available for histidine and Microcephaly
| Article | Year |
|---|---|
PRUNE1 c.933G>A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the literature.
Topics: Child; Exons; Histidine; Humans; Male; Microcephaly; Muscle Hypotonia; Pedigree; Phosphoric Monoester Hydrolases | 2022 |
1 other study(ies) available for histidine and Microcephaly
| Article | Year |
|---|---|
Microcephaly thin corpus callosum intellectual disability syndrome caused by mutated TAF2.
Topics: Chromosomes, Human, Pair 8; Computational Biology; Corpus Callosum; DNA Mutational Analysis; Family Health; Female; Histidine; Humans; Infant; Intellectual Disability; Magnetic Resonance Imaging; Male; Microcephaly; Mutation; Proline; TATA-Binding Protein Associated Factors; Transcription Factor TFIID | 2013 |