Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Pietra Greenberg"'
Publikováno v:
Endocrine Practice. 29:S35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::703819dbf4185f07a0857c055dc63943
https://doi.org/10.1016/s1530-891x(23)00146-5
https://doi.org/10.1016/s1530-891x(23)00146-5
Publikováno v:
Journal of the Endocrine Society. 6:A163-A164
Hypercalcemia is a relatively common clinical problem. Among all causes of hypercalcemia, primary hyperparathyroidism and malignancy are the most common. This case highlights the importance of collaboration between subspecialists to identify the etio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4302ec21103e48e1f3f36ccbaaa5353
https://doi.org/10.1210/jendso/bvac150.336
https://doi.org/10.1210/jendso/bvac150.336
Publikováno v:
Journal of the Endocrine Society. 6:A769-A769
MUTYH-associated polyposis (MAP) is an autosomal recessive syndrome caused by a mutation to the MUTYH gene, a base excision repair gene that repairs oxidative damage to DNA. Mutations to both allelic copies of this gene typically manifest as multiple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2fb540f2b415801bfd17d51d5313363
https://doi.org/10.1210/jendso/bvac150.1588
https://doi.org/10.1210/jendso/bvac150.1588
There are two common alleles at the Amylase-2 locus in populations of Gammarus palustris, the salt marsh amphipod. Intensive sampling of individuals from two localities at Jamaica Bay revealed a consistent pattern of heterozygote deficiency.ߝFive po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb10aec54667bf1b7e4faa472e1eaf89
https://europepmc.org/articles/PMC1202645/
https://europepmc.org/articles/PMC1202645/
