Zobrazeno 1 - 10
of 515
pro vyhledávání: '"developmental anomalies"'
Publikováno v:
口腔疾病防治, Vol 31, Iss 5, Pp 370-374 (2023)
Ankylosis of primary molars is a kind of eruption abnormality of the teeth, where the periodontal membrane disappears, owing to a bony union between bone and root. Studies have shown that the common proportion of ankylosed primary molars is 1.3%~8.9%
Externí odkaz:
https://doaj.org/article/0a1a625ff29f45eda40626398ce1db9b
Publikováno v:
PeerJ, Vol 11, p e16011 (2023)
In the literature there are numerous reports of developmental deformities in arthropods collected in their natural habitat. Since such teratogenically affected individuals are found purely by chance, the causes of their defects are unknown. Numerous
Externí odkaz:
https://doaj.org/article/7535a74e33df4e139dbba26afd71ba7b
Publikováno v:
Нижневолжский археологический вестник, Vol 21, Iss 2, Pp 100-119 (2022)
Introduction. Currently, the picture characterizing the health status of the population, inhabiting the Southern Urals during the Bronze Age, is fragmentary due to the unsystematic nature of paleopathological studies and the often small sizes or poor
Externí odkaz:
https://doaj.org/article/a3d70d5d463b4e77a992a2ff082dc7b4
Autor:
Sarfaraz Jalil Baig, Pallawi Priya
Publikováno v:
Journal of Minimal Access Surgery, Vol 19, Iss 1, Pp 144-146 (2023)
Ciliated foregut cysts (CFCs) are rare anomalies of the foregut epithelium. The common sites in the abdomen are liver and gall bladder. There are only 16 cases of CFC reported in the gall bladder to date. A 20-year-old girl presented with pain in the
Externí odkaz:
https://doaj.org/article/450422dc64684c3a977b9886b4bf0928
Publikováno v:
Indian Journal of Radiology and Imaging, Vol 32, Iss 03, Pp 355-364 (2022)
Inferior vena cava (IVC) can be involved by a wide gamut of developmental anomalies owing to its complex embryogenesis. Developmental anomalies of the IVC are not infrequent, seen in approximately 8.7% of the general population. Although most of the
Externí odkaz:
https://doaj.org/article/c623b354cca44c92a91604aefec9b4d7
Autor:
Frédéric Tran Mau-Them, Alexis Overs, Ange-Line Bruel, Romain Duquet, Mylene Thareau, Anne-Sophie Denommé-Pichon, Antonio Vitobello, Arthur Sorlin, Hana Safraou, Sophie Nambot, Julian Delanne, Sebastien Moutton, Caroline Racine, Camille Engel, Melchior De Giraud d’Agay, Daphne Lehalle, Alice Goldenberg, Marjolaine Willems, Christine Coubes, David Genevieve, Alain Verloes, Yline Capri, Laurence Perrin, Marie-Line Jacquemont, Laetitia Lambert, Elodie Lacaze, Julien Thevenon, Nadine Hana, Julien Van-Gils, Charlotte Dubucs, Varoona Bizaoui, Marion Gerard-Blanluet, James Lespinasse, Sandra Mercier, Anne-Marie Guerrot, Isabelle Maystadt, Emilie Tisserant, Laurence Faivre, Christophe Philippe, Yannis Duffourd, Christel Thauvin-Robinet
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Exome sequencing has a diagnostic yield ranging from 25% to 70% in rare diseases and regularly implicates genes in novel disorders. Retrospective data reanalysis has demonstrated strong efficacy in improving diagnosis, but poses organiz
Externí odkaz:
https://doaj.org/article/c14e4795329344a3bad7a62c2a7011bd