Cri du Chat syndrome.
Cerruti Mainardi P.
Orphanet J Rare Dis. 2006 Sep 5;1:33. doi: 10.1186/1750-1172-1-33.
Cri du chat syndrome: a critical review.
Rodríguez-Caballero A, Torres-Lagares D, Rodríguez-Pérez A, Serrera-Figallo MA, Hernández-Guisado JM, Machuca-Portillo G.
Med Oral Patol Oral Cir Bucal. 2010 May 1;15(3):e473-8. doi: 10.4317/medoral.15.e473.
Cri-du-chat syndrome.
Nandhagopal R, Udayakumar AM.
Indian J Med Res. 2014 Oct;140(4):570-1.
Cri-du-chat syndrome.
Chang CY, Lin SP, Lin HY, Chen YJ, Kao HA, Yeung CY, Hsu CH, Chi H.
Acta Paediatr Taiwan. 2007 Nov-Dec;48(6):328-31.
Cri-du-chat.
Sigafoos J, O'Reilly MF, Lancioni GE.
Dev Neurorehabil. 2009 Jun;12(3):119-21. doi: 10.1080/17518420902975720.
Cri du chat syndrome patients have DNA methylation changes in genes linked to symptoms of the disease.
Holland P, Wildhagen M, Istre M, Reiakvam OM, Dahl JA, Søraas A.
Clin Epigenetics. 2022 Oct 14;14(1):128. doi: 10.1186/s13148-022-01350-3.
A systematic review of the oral and craniofacial manifestations of cri du chat syndrome.
Corcuera-Flores JR, Casttellanos-Cosano L, Torres-Lagares D, Serrera-Figallo MÁ, Rodríguez-Caballero Á, Machuca-Portillo G.
Clin Anat. 2016 Jul;29(5):555-60. doi: 10.1002/ca.22654. Epub 2015 Dec 21.
Retinopathy in a Full-Term Infant with Cri-du-Chat Syndrome.
Chhaya N, Chan T.
R I Med J (2013). 2021 Feb 1;104(1):37-39.
Cri du chat syndrome: genotype-phenotype correlations and recommendations for clinical management.
Cornish K, Bramble D.
Dev Med Child Neurol. 2002 Jul;44(7):494-7. doi: 10.1017/s0012162201002419.
Cri du Chat syndrome: Characteristics of 73 Brazilian patients.
Honjo RS, Mello CB, Pimenta LSE, Nuñes-Vaca EC, Benedetto LM, Khoury RBF, Befi-Lopes DM, Kim CA.
J Intellect Disabil Res. 2018 Jun;62(6):467-473. doi: 10.1111/jir.12476. Epub 2018 Feb 20.
