Author:
Ibrahim Abdulla,Kirby Gail,Hardy Carol,Dias Renuka P,Tee Louise,Lim Derek,Berg Jonathan,MacDonald Fiona,Nightingale Peter,Maher Eamonn R
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Developmental Biology,Genetics,Molecular Biology
Reference30 articles.
1. Azzi S, Abi Habib W, Netchine I: Beckwith-Wiedemann and Russell-Silver Syndromes: from new molecular insights to the comprehension of imprinting regulation. Curr Opin Endocrinol Diabetes Obes. 2014, 21: 30-38. 10.1097/MED.0000000000000037.
2. Choufani S, Shuman C, Weksberg R: Molecular findings in Beckwith-Wiedemann syndrome. Am J Med Genet C: Semin Med Genet. 2013, 163C: 131-140.
3. Eggermann T, Algar E, Lapunzina P, Mackay D, Maher ER, Mannens M, Netchine I, Prawitt D, Riccio A, Temple IK, Weksberg R: Clinical utility gene card for: Beckwith-Wiedemann syndrome. Eur J Hum Genet. 2014, 22: doi:10.1038/ejhg.2013.132
4. Lim DH, Maher ER: Human imprinting syndromes. Epigenomics. 2009, 1: 347-369. 10.2217/epi.09.24.
5. Ishida M, Moore GE: The role of imprinted genes in humans. Mol Aspects Med. 2013, 34: 826-840. 10.1016/j.mam.2012.06.009.
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