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Gordon syndrome 相关文献:
The Molecular Genetics of Gordon Syndrome.
Mabillard H, Sayer JA.
Genes (Basel). 2019 Nov 29;10(12):986. doi: 10.3390/genes10120986.
PMID:31795491
Gordon Syndrome: a continuing story.
O'Shaughnessy KM.
Pediatr Nephrol. 2015 Nov;30(11):1903-8. doi: 10.1007/s00467-014-2956-7. Epub 2014 Dec 11.
PMID:25503323
[Gordon syndrome].
Sato R, Tujino M, Hirata Y.
Nihon Rinsho. 2000 Feb;58 Suppl 2:672-4.
PMID:11028425
Familial Gordon syndrome associated with a PIEZO2 mutation.
Alisch F, Weichert A, Kalache K, Paradiso V, Longardt AC, Dame C, Hoffmann K, Horn D.
Am J Med Genet A. 2017 Jan;173(1):254-259. doi: 10.1002/ajmg.a.37997. Epub 2016 Oct 7.
PMID:27714920
A Spanish Family with Gordon Syndrome Due to a Variant in the Acidic Motif of WNK1.
Peces R, Peces C, Espinosa L, Mena R, Blanco C, Tenorio-Castaño J, Lapunzina P, Nevado J.
Genes (Basel). 2023 Sep 27;14(10):1878. doi: 10.3390/genes14101878.
PMID:37895227
Gordon syndrome: literature review and a report of two cases.
Botha SJ, Bütow KW.
Cleft Palate Craniofac J. 2015 Jan;52(1):e18-22. doi: 10.1597/13-075.
PMID:24878349
ANKRD17-Related Neurodevelopmental Syndrome.
Sveden A, Gordon CT, Amiel J, Chopra M.
2022 Dec 22. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID:36548456
Gordon syndrome: Dental implications and a case report.
Roomaney IA, Walters J, Spencer C, Chetty M.
Spec Care Dentist. 2021 Nov;41(6):727-734. doi: 10.1111/scd.12615. Epub 2021 May 26.
PMID:34038001
Low-Renin Hypertension.
Athimulam S, Lazik N, Bancos I.
Endocrinol Metab Clin North Am. 2019 Dec;48(4):701-715. doi: 10.1016/j.ecl.2019.08.003. Epub 2019 Sep 25.
PMID:31655771
Gordon syndrome caused by a CUL3 mutation in a patient with short stature in Korea: a case report.
Park JH, Kim JH, Ahn YH, Kang HG, Ha IS, Cheong HI.
J Pediatr Endocrinol Metab. 2021 Sep 6;35(2):253-257. doi: 10.1515/jpem-2021-0361. Print 2022 Feb 23.
PMID:34480842
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