Dissanayake VH - Search Results

1

Post-zygotic breakage of a dicentric chromosome results in mosaicism for a telocentric 9p marker chromosome in a boy with developmental delay.

Pedurupillay CR, Misceo D, Gamage TH, Dissanayake VH, Frengen E. Pedurupillay CR, et al. Among authors: dissanayake vh. Gene. 2014 Jan 1;533(1):403-10. doi: 10.1016/j.gene.2013.09.090. Epub 2013 Oct 2. Gene. 2014. PMID: 24095780

2

A child with mosaicism for deletion (14)(q11.2q13).

Gamage TH, Godapitiya IU, Nanayakkara S, Jayasekara RW, Dissanayake VH. Gamage TH, et al. Among authors: dissanayake vh. Indian J Hum Genet. 2012 Jan;18(1):130-3. doi: 10.4103/0971-6866.96684. Indian J Hum Genet. 2012. PMID: 22754240 Free PMC article.

3

A Sri Lankan child with 49,XXXXY syndrome.

Dissanayake VH, Bandarage P, Pedurupillay CR, Jayasekara RW. Dissanayake VH, et al. Indian J Hum Genet. 2010 Sep;16(3):164-5. doi: 10.4103/0971-6866.73413. Indian J Hum Genet. 2010. PMID: 21206706 Free PMC article.

4

An infant born to a mother with gestational diabetes presenting with 49,XXXXY syndrome and renal agenesis-a case report.

Sumathipala D, Gamage T, Wijesiriwardena B, Jayasekara RW, Dissanayake VH. Sumathipala D, et al. Among authors: dissanayake vh. J Clin Res Pediatr Endocrinol. 2012 Dec;4(4):223-5. doi: 10.4274/jcrpe.764. Epub 2012 Oct 2. J Clin Res Pediatr Endocrinol. 2012. PMID: 23032147 Free PMC article.

5

17p11.2 and Xq28 duplication detected in a girl diagnosed with Potocki-Lupski syndrome.

Sumathipala DS, Mandawala EN, Sumanasena SP, Dissanayake VH. Sumathipala DS, et al. Among authors: dissanayake vh. BMC Res Notes. 2015 Sep 29;8:506. doi: 10.1186/s13104-015-1439-7. BMC Res Notes. 2015. PMID: 26419729 Free PMC article.

6

Child with deletion 9p syndrome presenting with craniofacial dysmorphism, developmental delay, and multiple congenital malformations.

Sirisena ND, Wijetunge UK, de Silva R, Dissanayake VH. Sirisena ND, et al. Among authors: dissanayake vh. Case Rep Genet. 2013;2013:785830. doi: 10.1155/2013/785830. Epub 2013 Jul 25. Case Rep Genet. 2013. PMID: 23984121 Free PMC article.

7

Angelman syndrome presenting with a rare seizure type in a patient with 15q11.2 deletion: a case report.

Ranasinghe JC, Chandradasa D, Fernando S, Kodithuwakku U, Mandawala DE, Dissanayake VH. Ranasinghe JC, et al. Among authors: dissanayake vh. J Med Case Rep. 2015 Jun 16;9:142. doi: 10.1186/s13256-015-0622-8. J Med Case Rep. 2015. PMID: 26077608 Free PMC article.

8

Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature.

Mishra R, Paththinige CS, Sirisena ND, Nanayakkara S, Kariyawasam UGIU, Dissanayake VHW. Mishra R, et al. BMC Pediatr. 2018 Jan 8;18(1):4. doi: 10.1186/s12887-017-0980-z. BMC Pediatr. 2018. PMID: 29310616 Free PMC article. Review.

9

A Sri Lankan child with 48,XXXX syndrome.

Padeniya PM, Godapitiya I, Pathirana DR, Jayasekara RW, Dissanayake VH. Padeniya PM, et al. Among authors: dissanayake vh. Indian J Pediatr. 2014 Feb;81(2):201-2. doi: 10.1007/s12098-013-0995-x. Epub 2013 Mar 14. Indian J Pediatr. 2014. PMID: 23494840 No abstract available.

10

The low frequency of Y chromosome microdeletions in subfertile males in a Sinhalese population of Sri Lanka.

Wettasinghe TK, Jayasekara RW, Dissanayake VH. Wettasinghe TK, et al. Among authors: dissanayake vh. Indian J Hum Genet. 2012 Sep;18(3):320-5. doi: 10.4103/0971-6866.107985. Indian J Hum Genet. 2012. PMID: 23716940 Free PMC article.

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