In vitro evaluation of pro-apoptotic and anti-metastatic activity of Oliveria decumbens vent. extract, an endemic Persian medicinal plant, on HT-29 colorectal cancer cell line von Khodavirdipour, Amir, Haddadi, Fatemeh, Rouhani nejad, Hamideh, Shiri, Yasoub, Preetha Tilak, Veronica

Volltext

Rare cryptic translocation seen acute myeloid leukemia – A case report von Subramaniam, Amudha, Metilda, Raina, Tilak, Preetha

Volltext

Prevalence of 7q deletion in patients with Acute myeloid leukemia von shastry, anjali, Subramaniam, Amudha, Tilak, Preetha

Volltext

Cytogenetic Abnormalities Identified in Cases of Amenorrhea von Vijay, Christy, Amudha, S, Tilak, Preetha, Margaret, Mary, Raina, P

Volltext

Genetic Mutations Reported in Patients of Consanguineous and Nonconsanguineous Marriages who Presented at a Tertiary Health Center for Genetic Counseling von Vijay, Christy, Ramesh, Naveen, Joseph, Abhay, Tilak, Preetha, Thanmayi, GS

Volltext

APPLICATION OF KARYOTYPING AND FLOURESCENT IN SITU HYBRIDISATION IN DETECTION OF KLINEFELTER SYNDROME von Shastry, Anjali, Tilak, Preetha, Subramaniam, Amudha

Volltext

Functional characterization of novel variants in SMPD1 in Indian patients with acid sphingomyelinase deficiency von Deshpande, Dipti, Gupta, Shailesh Kumar, Sarma, Asodu Sandeep, Ranganath, Prajnya, Jain S., Jamal Md Nurul, Sheth, Jayesh, Mistri, Mehul, Gupta, Neerja, Kabra, Madhulika, Phadke, Shubha R., Girisha, Katta M., Dua Puri, Ratna, Aggarwal, Shagun, Datar, Chaitanya, Mandal, Kausik, Tilak, Preetha, Muranjan, Mamta, Bijarnia‐Mahay, Sunita, Rama Devi A., Radha, Tayade, Naresh B., Ranjan, Akash, Dalal, Ashwin B.

Volltext

Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patients von Ganapathy, Aparna, Mishra, Avshesh, Soni, Megha Rani, Kumar, Priyanka, Sadagopan, Mukunth, Kanthi, Anil Vittal, Patric, Irene Rosetta Pia, George, Sobha, Sridharan, Aparajit, Thyagarajan, T. C., Aswathy, S. L., Vidya, H. K., Chinnappa, Swathi M., Nayanala, Swetha, Prakash, Manasa B., Raghavendrachar, Vijayashree G., Parulekar, Minothi, Gowda, Vykuntaraju K., Nampoothiri, Sheela, Menon, Ramshekhar N., Pachat, Divya, Udani, Vrajesh, Naik, Neeta, Kamate, Mahesh, Devi, A. Radha Rama, Mohammed Kunju, P. A., Nair, Mohandas, Hegde, Anaita Udwadia, Kumar, M. Pradeep, Sundaram, Soumya, Tilak, Preetha, Puri, Ratna D., Shah, Krati, Sheth, Jayesh, Hasan, Qurratulain, Sheth, Frenny, Agrawal, Pooja, Katragadda, Shanmukh, Veeramachaneni, Vamsi, Chandru, Vijay, Hariharan, Ramesh, Mannan, Ashraf U.

Volltext

Spectrum of SMPD1 mutations in Asian-Indian patients with acid sphingomyelinase (ASM)-deficient Niemann-Pick disease von Ranganath, Prajnya, Matta, Divya, Bhavani, Gandham SriLakshmi, Wangnekar, Savita, Jain, Jamal Mohammed Nurul, Verma, Ishwar C., Kabra, Madhulika, Puri, Ratna Dua, Danda, Sumita, Gupta, Neerja, Girisha, Katta M., Sankar, Vaikom H., Patil, Siddaramappa J., Ramadevi, Akella Radha, Bhat, Meenakshi, Gowrishankar, Kalpana, Mandal, Kausik, Aggarwal, Shagun, Tamhankar, Parag Mohan, Tilak, Preetha, Phadke, Shubha R., Dalal, Ashwin

Volltext

Embryogenesis and types of subcostal hernia—A rare entity von Raghu, S.R, Alladi, Anand, Vepakomma, Deepti, Siddappa, O.S, Tilak, Preetha

Volltext

Spectrum of mutations in the SMPD1 gene in Asian Indian patients with acid sphingomyelinase deficient Niemann–Pick disease von Ranganath, Prajnya, Matta, Divya, Bhavani, Gandham SriLakshmi, Wangnekar, Savita, Jain, Jamal Mohammed Nurul, Verma, Ishwar C., Kabra, Madhulika, Puri, Ratna D., Danda, Sumita, Gupta, Neerja, Girisha, Katta M., Sankar, Vaikom H., Patil, Siddaramappa J., Devi, Akella Radha Rama, Bhat, Meenakshi, Gowrishankar, Kalpana, Mandal, Kausik, Aggarwal, Shagun, Tamhankar, Parag Mohan, Tilak, Preetha, Phadke, Shubha R., Dalal, Ashwin

Volltext

Three decades of turner`s syndrome–An experience from a South Indian genetic center von Abdul Mateen Athar, Jyothi Idiculla, Seby John, Preetha Tilak, Rahul Kapur

Volltext

Karyotyping and counseling in bad obstetric history and infertility von Sayee Rajangam, Preetha Tilak, Aruna N, Rema Devi

Volltext

A novel mutation 5’ to the HMG box of theSRY gene in a case of Swyer syndrome von Saifi, G. Mustafa, Tilak, Preetha, Veitia, Reiner, Thomas, I. Manorama, Tharapel, Avirachan, Mcelreavey, Ken, Fellous, Mark, Chandra, H. Sharat

Volltext

An unusual case of haemophilia--a case report von Sitalakshmi, S, Tilak, P, Srikrishna, A, Damodar, P, Thomas, I M

Volltext

Klinefelter Syndrome - Cytogenetic Findings von Thomas, I.M., Hedge, Sridevi, Tilak, Preetha, Lincoln, Shavanthi, Joseph, Ann, Jagannath, Mythili, Rajangam, Sayee

Volltext

sY116, a human Y-linked polymorphic STS von Saifi, G. Mustafa, Veitia, Reiner, El Khil, Houssein Khodjet, Barbaux, Sandrine, Tilak, Preetha, Thomas, I. Manorama, Fellous, Marc

Volltext