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Year | Number of Results |
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2020 | 1 |
2022 | 1 |
2023 | 3 |
2024 | 1 |
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Page 1
Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study.
Neuropediatrics. 2023 Aug;54(4):225-238. doi: 10.1055/a-2034-8528. Epub 2023 Feb 14.
Neuropediatrics. 2023.
PMID: 36787800
A New Variant of the IER3IP1 Gene: The First Case of Microcephaly, Epilepsy, and Diabetes Syndrome 1 from Turkey.
Söbü E, Kaya Özçora GD, Yılmaz Güleç E, Şahinoğlu B, Tahmiscioğlu Bucak F.
Söbü E, et al. Among authors: sahinoglu b.
J Clin Res Pediatr Endocrinol. 2022 Nov 23. doi: 10.4274/jcrpe.galenos.2022.2022-8-12. Online ahead of print.
J Clin Res Pediatr Endocrinol. 2022.
PMID: 36416459
Free article.
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Lathosterolosis: a rare cholesterol metabolism disorder with a wide range of clinical variability.
Söbü E, Kaya Özçora GD, Görükmez Ö, Şahinoğlu B.
Söbü E, et al. Among authors: sahinoglu b.
J Pediatr Endocrinol Metab. 2023 Jan 6;36(4):424-429. doi: 10.1515/jpem-2022-0586. Print 2023 Apr 25.
J Pediatr Endocrinol Metab. 2023.
PMID: 36607840
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Coexistence of Bloom Syndrome and Kostmann Disease and a Novel Mutation.
Pekpak Sahinoglu E, Oren AC, Sahinoglu B, Gumus U, Akbayram S.
Pekpak Sahinoglu E, et al. Among authors: sahinoglu b.
J Pediatr Hematol Oncol. 2024 Mar 1;46(2):e199-e201. doi: 10.1097/MPH.0000000000002798. Epub 2023 Dec 18.
J Pediatr Hematol Oncol. 2024.
PMID: 38113221
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Autosomal recessive Robinow syndrome with novel ROR2 variants: distinct cases exhibiting the clinical variability.
Kirat E, Mutlu Albayrak H, Sahinoglu B, Gurler AI, Karaer K.
Kirat E, et al. Among authors: sahinoglu b.
Clin Dysmorphol. 2020 Jul;29(3):137-140. doi: 10.1097/MCD.0000000000000319.
Clin Dysmorphol. 2020.
PMID: 32195677
No abstract available.
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