Correspondence

Springer Science and Business Media LLC - Tập 12 - Trang 374-375 - 2016
Nirmala Sirisena1, Vajira H.W. Dissanayake1
1Human Genetics Unit, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka

Tài liệu tham khảo

Thillainathan S, Sirisena ND, Kariyawasam KW, Jayasekara RW, Dissanayake VH. Cytogenetic analysis of chromosomal abnormalities in Sri Lankan children. World J Pediatr 2015;11:374–379.

Pedurupillay CR1, Misceo D, Gamage TH, Dissanayake VH, Frengen E. Gene. Post-zygotic breakage of a dicentric chromosome results in mosaicism for a telocentric 9p marker chromosome in a boy with developmental delay. Gene 2014;533:403–410.

Gamage TH1, Godapitiya IU, Nanayakkara S, Jayasekara RW, Dissanayake VH. A child with mosaicism for deletion (14) (q11. 2q13). Indian J Hum Genet 2012;18:130–133.

Dissanayake VH, Bandarage P, Pedurupillay CR, Jayasekara RW. A Sri Lankan child with 49, XXXXY syndrome. Indian J Hum Genet 2010;16:164–165.

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Springer Science and Business Media LLC

Tập 12

374-375

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