Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nidhi Bhoyar"'
Publikováno v:
Contemporary Clinical Dentistry, Vol 11, Iss 4, Pp 395-398 (2020)
Pycnodysostosis is an autosomal recessive, rare genetic osteosclerotic disorder that caused by mutation in gene coding for Cathepsin K. The bones in pycnodysostosis are abnormally dense and brittle because of insufficient reabsorption process. This s
Externí odkaz:
https://doaj.org/article/b907e05fb3cf4e87acc292be4c930971
Publikováno v:
Contemporary Clinical Dentistry, Vol 7, Iss 4, Pp 558-561 (2016)
Tuberous sclerosis complex (TSC) is a rare multisystem genetic disease, with an estimated incidence of 1 in 6000–1 in 10,000. TSC is an autosomal dominant syndrome involving heart, kidneys, lungs, and skin. The classic triad of TSC is seizures, men
Externí odkaz:
https://doaj.org/article/bc40ec94eed3455bb55278ce2f824998
Publikováno v:
Contemporary Clinical Dentistry
Contemporary Clinical Dentistry, Vol 11, Iss 4, Pp 395-398 (2020)
Contemporary Clinical Dentistry, Vol 11, Iss 4, Pp 395-398 (2020)
Pycnodysostosis is an autosomal recessive, rare genetic osteosclerotic disorder that caused by mutation in gene coding for Cathepsin K. The bones in pycnodysostosis are abnormally dense and brittle because of insufficient reabsorption process. This s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40400bd71f6025a61dae38088155d514
http://europepmc.org/articles/PMC8035836
http://europepmc.org/articles/PMC8035836
Publikováno v:
Contemporary Clinical Dentistry
Contemporary Clinical Dentistry, Vol 7, Iss 4, Pp 558-561 (2016)
Contemporary Clinical Dentistry, Vol 7, Iss 4, Pp 558-561 (2016)
Tuberous sclerosis complex (TSC) is a rare multisystem genetic disease, with an estimated incidence of 1 in 6000–1 in 10,000. TSC is an autosomal dominant syndrome involving heart, kidneys, lungs, and skin. The classic triad of TSC is seizures, men
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57b94d4536536d139f085b3782243967
https://doi.org/10.4103/0976-237x.194120
https://doi.org/10.4103/0976-237x.194120