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Page 1
POGZ truncating alleles cause syndromic intellectual disability.
Genome Med. 2016 Jan 6;8(1):3. doi: 10.1186/s13073-015-0253-0.
Genome Med. 2016.
PMID: 26739615
Free PMC article.
A multidisciplinary approach to the clinical management of Prader-Willi syndrome.
Duis J, van Wattum PJ, Scheimann A, Salehi P, Brokamp E, Fairbrother L, Childers A, Shelton AR, Bingham NC, Shoemaker AH, Miller JL.
Duis J, et al. Among authors: fairbrother l.
Mol Genet Genomic Med. 2019 Mar;7(3):e514. doi: 10.1002/mgg3.514. Epub 2019 Jan 29.
Mol Genet Genomic Med. 2019.
PMID: 30697974
Free PMC article.
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Congenital Arthrogryposis: An Extension of the 15q11.2 BP1-BP2 Microdeletion Syndrome?
Usrey KM, Williams CA, Dasouki M, Fairbrother LC, Butler MG.
Usrey KM, et al. Among authors: fairbrother lc.
Case Rep Genet. 2014;2014:127258. doi: 10.1155/2014/127258. Epub 2014 Feb 12.
Case Rep Genet. 2014.
PMID: 24778887
Free PMC article.
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Biomineralization of gold in biofilms of Cupriavidus metallidurans.
Fairbrother L, Etschmann B, Brugger J, Shapter J, Southam G, Reith F.
Fairbrother L, et al.
Environ Sci Technol. 2013 Mar 19;47(6):2628-35. doi: 10.1021/es302381d. Epub 2013 Mar 4.
Environ Sci Technol. 2013.
PMID: 23405956
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Mild Angelman syndrome phenotype due to a mosaic methylation imprinting defect.
Fairbrother LC, Cytrynbaum C, Boutis P, Buiting K, Weksberg R, Williams C.
Fairbrother LC, et al.
Am J Med Genet A. 2015 Jul;167(7):1565-9. doi: 10.1002/ajmg.a.37058. Epub 2015 Apr 21.
Am J Med Genet A. 2015.
PMID: 25899869
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Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia.
Nguyen TTM, Murakami Y, Sheridan E, Ehresmann S, Rousseau J, St-Denis A, Chai G, Ajeawung NF, Fairbrother L, Reimschisel T, Bateman A, Berry-Kravis E, Xia F, Tardif J, Parry DA, Logan CV, Diggle C, Bennett CP, Hattingh L, Rosenfeld JA, Perry MS, Parker MJ, Le Deist F, Zaki MS, Ignatius E, Isohanni P, Lönnqvist T, Carroll CJ, Johnson CA, Gleeson JG, Kinoshita T, Campeau PM.
Nguyen TTM, et al. Among authors: fairbrother l.
Am J Hum Genet. 2017 Nov 2;101(5):856-865. doi: 10.1016/j.ajhg.2017.09.020.
Am J Hum Genet. 2017.
PMID: 29100095
Free PMC article.
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