Imprinting disorders in humans: a review.
Butler MG.
Curr Opin Pediatr. 2020 Dec;32(6):719-729. doi: 10.1097/MOP.0000000000000965.
Beckwith Weidemann Syndrome.
Raju U, Dhulia A, Sharma M.
Med J Armed Forces India. 2004 Jan;60(1):69-70. doi: 10.1016/S0377-1237(04)80165-5. Epub 2011 Jul 21.
Mesothelial Inclusion Cyst in an Infant with Beckwith-Weidemann Syndrome.
Lehane AJ, Rauh J, Sieren LM.
Am Surg. 2023 Aug;89(8):3616-3617. doi: 10.1177/00031348231167408. Epub 2023 Mar 27.
Beckwith-Weidemann syndrome with IC2 (KvDMR1) hypomethylation defect: a novel mutation.
Pandita A, Gupta S, Gupta G, Panghal A.
BMJ Case Rep. 2018 Mar 30;2018:bcr2017222419. doi: 10.1136/bcr-2017-222419.
Beckwith Weidemann syndrome: a behavioral phenotype-genotype study.
Kent L, Bowdin S, Kirby GA, Cooper WN, Maher ER.
Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1295-7. doi: 10.1002/ajmg.b.30729.
Diazoxide therapy in the syndrome of Beckwith-Weidemann-Coombs.
Gotlin RW.
J Pediatr. 1973 Aug;83(2):342-3. doi: 10.1016/s0022-3476(73)80509-8.
Tongue reduction in Beckwith-Weidemann syndrome.
Kacker A, Honrado C, Martin D, Ward R.
Int J Pediatr Otorhinolaryngol. 2000 Jun 9;53(1):1-7. doi: 10.1016/s0165-5876(00)00280-9.
Childhood cancers: hepatoblastoma.
Herzog CE, Andrassy RJ, Eftekhari F.
Oncologist. 2000;5(6):445-53. doi: 10.1634/theoncologist.5-6-445.
Erratum: Anaesthetic considerations in an infant with Beckwith-Weidemann syndrome and hepatoblastoma for partial hepatectomy: Erratum.
[No authors listed]
Indian J Anaesth. 2015 Mar;59(3):205. doi: 10.4103/0019-5049.153052.
DNA methylation in genomic imprinting.
Tycko B.
Mutat Res. 1997 Apr;386(2):131-40. doi: 10.1016/s1383-5742(96)00049-x.
