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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 1
1995 1
2008 2
2009 1
2010 1
2011 1
2021 1
2022 0
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7 results
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Page 1
Beckwith Weidemann syndrome: a behavioral phenotype-genotype study.
Kent L, Bowdin S, Kirby GA, Cooper WN, Maher ER. Kent L, et al. Among authors: kirby ga. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1295-7. doi: 10.1002/ajmg.b.30729. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18314872
Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism.
Cangul H, Morgan NV, Forman JR, Saglam H, Aycan Z, Yakut T, Gulten T, Tarim O, Bober E, Cesur Y, Kirby GA, Pasha S, Karkucak M, Eren E, Cetinkaya S, Bas V, Demir K, Yuca SA, Meyer E, Kendall M, Hogler W, Barrett TG, Maher ER. Cangul H, et al. Among authors: kirby ga. Clin Endocrinol (Oxf). 2010 Nov;73(5):671-7. doi: 10.1111/j.1365-2265.2010.03849.x. Clin Endocrinol (Oxf). 2010. PMID: 20718767
Food intolerance and Crohn's disease.
Riordan AM, Rucker JT, Kirby GA, Hunter JO. Riordan AM, et al. Among authors: kirby ga. Gut. 1994 Apr;35(4):571-2. doi: 10.1136/gut.35.4.571-b. Gut. 1994. PMID: 8175004 Free PMC article. No abstract available.
Loss-of-function mutations in RAB18 cause Warburg micro syndrome.
Bem D, Yoshimura S, Nunes-Bastos R, Bond FC, Kurian MA, Rahman F, Handley MT, Hadzhiev Y, Masood I, Straatman-Iwanowska AA, Cullinane AR, McNeill A, Pasha SS, Kirby GA, Foster K, Ahmed Z, Morton JE, Williams D, Graham JM, Dobyns WB, Burglen L, Ainsworth JR, Gissen P, Müller F, Maher ER, Barr FA, Aligianis IA. Bem D, et al. Among authors: kirby ga. Am J Hum Genet. 2011 Apr 8;88(4):499-507. doi: 10.1016/j.ajhg.2011.03.012. Am J Hum Genet. 2011. PMID: 21473985 Free PMC article.