Sabita K. Murthy
Department of Genetics
Al Wasl Hospital
Department of Health and Medical Services
Dubai
UAE
Name/email consistency: high
- Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) de novo in a child with dysmorphic features and streaky pigmentation: case report. Murthy, S.K., Malhotra, A.K., Jacob, P.S., Naveed, S., Al-Rowaished, E.E., Mani, S., Padariyakam, S., Pramathan, R., Nath, R., Al-Ali, M.T., Al-Gazali, L. Molecular. Cytogenetics (2008)
- Incidence of Down syndrome in Dubai, UAE. Murthy, S.K., Malhotra, A.K., Mani, S., Shara, M.E., Al-Rowaished, E.E., Naveed, S., Alkhayat, A.I., Alali, M.T. Med. Princ. Pract (2007)
- Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment. Murthy, S.K., Nygren, A.O., El Shakankiry, H.M., Schouten, J.P., Al Khayat, A.I., Ridha, A., Al Ali, M.T. Cytogenet. Genome Res. (2007)









