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23.12.2020 · Our findings suggest that genetic tests are critical technique for diagnosis of GADEVS, especially in patients with early-childhood, unexplained ...
23.12.2020 · Gabriele-de Vries syndrome (GADEVS), also known as YY1 haploinsufficiency syndrome, is a very rare autosomal dominant neurodevelopmental ...
Weitere Fragen
... https://onlinelibrary.wiley.com/iucr/doi/10.1107/S2053229620007822 [dostęp: 08.07.2020] Charakt. formalna: ARZ Charakt. merytoryczna: ORG Afiliacja GUMed
from: https://onlinelibrary.wiley.com/doi/ full/10.1111/hel.12383. 15. Le Thi TG, Werkstetter K, Kotilea K, et al. Management of Helicobacter pylori.
... DOI: 2/9632. Tytuł oryginału: Comparison of ... https://onlinelibrary.wiley.com/iucr/doi/10.1107 ... Laub, Ruth-Ann M. Lee, Edgar Lerma, Rochelle Liverman, Angela Q ...
https://link.springer.com/article/10.1007%2Fs00439-015-1562-5 ... https://onlinelibrary.wiley.com/doi/abs/10.1002 ... doi: 10.1002/mgg3.1546.</dc:relation> <dc ...
Wiley Online Library, DOI: 10.1002/mgg3.320 Abstract; Giacopuzzi, E et al. (2017) Exome sequencing in schizophrenic patients with high levels of homozygosity ...
Distal myopathies are clinically, pathologically, and genetically heterogeneous. The age of onset ranges from childhood to late-adulthood. Muscle weakness can ...
Hoboken : Wiley. ISSN 2324-9269. 2023, vol. 11, no. 1, art. no. e2059, p. [1-6]. DOI: 10.1002/mgg3.2059. [DB: Science Citation Index Expanded (Web of ...
... de type 2 MH - Humains MH - Inhibiteurs du ... https://dx.doi.org/10.1177/10742484241233872 ER ... 10.1002/ehf2.14551 C1 - 20240127 MH - Défaillance cardiaque ...