https://orcid.org/0000-0002-6363-9202
References
- Verjaal M, De Nef J. A patient with a partial deletion of the short arm of chromosome 3: karyotype: 46, XY, del (3) (p25). Am J Dis Child. 1978;132(1):43–45. doi:10.1001/archpedi.1978.02120260045012.
- Fernandez T, Morgan T, Davis N, Klin A, Morris A, Farhi A, et al. Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome. Am J Hum Genet. 2008;82(6):1385. doi:10.1016/j.ajhg.2008.04.021.
- Kaur A, Khetarpal S. 3p deletion syndrome. Indian Pediatr. 2013;50:795–796.
- Mowrey PN, Chorney MJ, Venditti CP, Latif F, Modi WS, Lerman MI, et al. Clinical and molecular analyses of deletion 3p25-pter syndrome. Am J Med Genet. 1993;46(6):623–629. doi:10.1002/ajmg.1320460604.
- Martins M, Arantes R, Botelho P, Souto M, Moutinho O, Pinto Leite R. Familiar del3p syndrome: the uncertainty of the prognosis. A case report. Clin Case Rep. 2021;9(4):2365–2368. doi:10.1002/ccr3.4036.
- Moncla A, Philip N, Mattei JF. Blepharophimosis-mental retardation syndrome and terminal deletion of chromosome 3p. J Med Genet. 1995;32(3):245–246. doi:10.1136/jmg.32.3.245-a.
- Ali MJ, Mohapatra S, Mulay K, Naik MN, Honavar SG. Incomplete punctal canalisation: the external and internal punctal membranes. Outcomes of membranotomy and adjunctive procedures. Br J Ophthalmol. 2013;97(1):92–95. doi:10.1136/bjophthalmol-2012-302277.