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Monozygotic twins discordant for a congenital cranial dysinnervation disorder with features of Moebius syndrome.
Am J Med Genet A. 2023 Nov;191(11):2743-2748. doi: 10.1002/ajmg.a.63389. Epub 2023 Sep 7.
Am J Med Genet A. 2023.
PMID: 37675855
Variable clinical severity in TANGO2 deficiency: Case series and literature review.
Schymick J, Leahy P, Cowan T, Ruzhnikov MRZ, Gates R, Fernandez L, Pramanik G; Undiagnosed Diseases Network; Yarlagadda V, Wheeler M, Bernstein JA, Enns GM, Lee C.
Schymick J, et al.
Am J Med Genet A. 2022 Feb;188(2):473-487. doi: 10.1002/ajmg.a.62543. Epub 2021 Oct 19.
Am J Med Genet A. 2022.
PMID: 34668327
Review.
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Clinical, biochemical and genetic characteristics of MOGS-CDG: a rare congenital disorder of glycosylation.
Shimada S, Ng BG, White AL, Nickander KK, Turgeon C, Liedtke KL, Lam CT, Font-Montgomery E, Lourenco CM, He M, Peck DS, Umana LA, Uhles CL, Haynes D, Wheeler PG, Bamshad MJ, Nickerson DA, Cushing T, Gates R, Gomez-Ospina N, Byers HM; UW Center for Mendelian Genomics; Scalco FB, Martinez NN, Sachdev R, Smith L, Poduri A, Malone S, Harris RV, Scheffer IE, Rosenzweig SD, Adams DR, Gahl WA, Malicdan MCV, Raymond KM, Freeze HH, Wolfe LA.
Shimada S, et al.
J Med Genet. 2022 Jul 5:jmedgenet-2021-108177. doi: 10.1136/jmedgenet-2021-108177. Online ahead of print.
J Med Genet. 2022.
PMID: 35790351
Free PMC article.
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Medical genetics education for pediatrics residents: A brief report.
Gates RW, Hudgins L, Huffman LC.
Gates RW, et al.
Genet Med. 2022 Nov;24(11):2408-2412. doi: 10.1016/j.gim.2022.08.003. Epub 2022 Aug 27.
Genet Med. 2022.
PMID: 36029300
Free article.
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Novel variants in KAT6B spectrum of disorders expand our knowledge of clinical manifestations and molecular mechanisms.
Yabumoto M, Kianmahd J, Singh M, Palafox MF, Wei A, Elliott K, Goodloe DH, Dean SJ, Gooch C, Murray BK, Swartz E, Schrier Vergano SA, Towne MC, Nugent K, Roeder ER, Kresge C, Pletcher BA, Grand K, Graham JM Jr, Gates R, Gomez-Ospina N, Ramanathan S, Clark RD, Glaser K, Benke PJ, Cohen JS, Fatemi A, Mu W, Baranano KW, Madden JA, Gubbels CS, Yu TW, Agrawal PB, Chambers MK, Phornphutkul C, Pugh JA, Tauber KA, Azova S, Smith JR, O'Donnell-Luria A, Medsker H, Srivastava S, Krakow D, Schweitzer DN, Arboleda VA.
Yabumoto M, et al.
Mol Genet Genomic Med. 2021 Oct;9(10):e1809. doi: 10.1002/mgg3.1809. Epub 2021 Sep 14.
Mol Genet Genomic Med. 2021.
PMID: 34519438
Free PMC article.
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De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities.
Okur V, Chen Z, Vossaert L, Peacock S, Rosenfeld J, Zhao L, Du H, Calamaro E, Gerard A, Zhao S, Kelsay J, Lahr A, Mighton C, Porter HM, Siemon A, Silver J, Svihovec S, Fong CT, Grant CL, Lerner-Ellis J, Manickam K, Madan-Khetarpal S, McCandless SE, Morel CF, Schaefer GB, Berry-Kravis EM, Gates R, Gomez-Ospina N, Qiu G, Zhang TJ, Wu Z, Meng L, Liu P, Scott DA, Lupski JR, Eng CM, Wu N, Yuan B.
Okur V, et al.
NPJ Genom Med. 2021 Dec 7;6(1):104. doi: 10.1038/s41525-021-00268-8.
NPJ Genom Med. 2021.
PMID: 34876591
Free PMC article.
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Extramammary Paget's disease with diffuse involvement of the lower female genito-urinary system.
Geisler JP, Gates RW, Shirrell W, Parker SM, Maloney CD, Wiemann MC, Geisler HE.
Geisler JP, et al. Among authors: gates rw.
Int J Gynecol Cancer. 1997 Jan;7(1):84-7. doi: 10.1046/j.1525-1438.1997.00405.x.
Int J Gynecol Cancer. 1997.
PMID: 12795809
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Timing of extractions in orthodontia.
GATES RW.
GATES RW.
Aust J Dent. 1951 Oct;55(5):356-8.
Aust J Dent. 1951.
PMID: 14886259
No abstract available.
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