Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ramitha Enakshi Kumar S"'
Publikováno v:
National Board of Examinations Journal of Medical Sciences, Vol Volume 2, Iss Issue 8, Pp 819-824 (2024)
Background: A Wu type X-linked syndromic intellectual developmental disorder is caused by mutations in the GRIA3 gene This disorder is characterised by autistic features, hyporeflexia, intellectual disability and facial dysmorphism. Case report: The
Externí odkaz:
https://doaj.org/article/3caaabecb221408db8da11ef1f55d71e
Publikováno v:
Sri Lanka Journal of Child Health. 51:605
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffaba8ec838872eca4d2eaf7966d5d82
https://doi.org/10.4038/sljch.v51i4.10379
https://doi.org/10.4038/sljch.v51i4.10379
Autor:
P. Vahini, Ramitha Enakshi Kumar. S
Publikováno v:
INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH. :69-70
Objective: The objective of this study is to comprehensively put forth the anatomical variations in the origin and course of lingual and facial arteries found in adult cadavers. Methods: Ten human cadavers were dissected and studied for variations fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a32f668527b3e87cf7d3ee0b1f5817a
https://doi.org/10.36106/ijsr/9028507
https://doi.org/10.36106/ijsr/9028507