hyaluronoglucosaminidase has been researched along with Cleft Palate 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 |
---|---|
Banka, S; Baple, EL; Barker, E; Bhoj, E; Capasso, J; Chandler, KE; Chioza, BA; Coban-Akdemir, ZH; Crosby, AH; Farrow, EG; Fasham, J; Ghosh, P; Gunning, AC; Hakonarson, H; Hemming, R; Jackson, A; Keena, B; Kussman, J; Levin, AV; Li, D; Lin, S; Lupski, JR; Neuhann, TM; Onesimo, R; Osawa, N; Pizzi, S; Posey, JE; Radio, FC; Rawlins, LE; Rodriguez, MC; Sheppard, SE; Tartaglia, M; Thiffault, I; Triggs-Raine, B; Wenger, OK; Wentzensen, IM; Zackai, EH; Zahka, K; Zampino, G; Zhou, D | 1 |
Alkuraya, FS; Baple, EL; Behr, ER; Blakley, B; Chioza, BA; Chowdhury, B; Crosby, AH; Cross, HE; Cross, L; Dolinsky, V; Faqeih, E; Harlalka, GV; Hasan, SN; Ishida, M; Jackson, M; Lees, M; Mark, B; Muggenthaler, MM; Patton, MA; Salter, C; Sharma, S; Stanier, P; Triggs-Raine, B; Zahka, K | 1 |
2 other study(ies) available for hyaluronoglucosaminidase and Cleft Palate
Article | Year |
---|---|
Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency.
Topics: Alleles; Animals; Cell Adhesion Molecules; Cleft Lip; Cleft Palate; Genetic Association Studies; GPI-Linked Proteins; Humans; Hyaluronoglucosaminidase; Mice; Phenotype | 2022 |
Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice.
Topics: Adolescent; Animals; Cell Adhesion Molecules; Child; Child, Preschool; Cleft Lip; Cleft Palate; Cor Triatriatum; Female; GPI-Linked Proteins; Humans; Hyaluronoglucosaminidase; Male; Mice; Mice, Inbred C57BL; Mutation; Pedigree; Penetrance; Syndrome | 2017 |