Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity von Bachmann-Gagescu, R, Dempsey, J C, Phelps, I G, O'Roak, B J, Knutzen, D M, Rue, T C, Ishak, G E, Isabella, C R, Gorden, N, Adkins, J, Boyle, E A, de Lacy, N, O'Day, D, Alswaid, A, Ramadevi A, Radha, Lingappa, L, Lourenço, C, Martorell, L, Garcia-Cazorla, À, Ozyürek, H, Haliloğlu, G, Tuysuz, B, Topçu, M, Chance, P, Parisi, M A, Glass, I A, Shendure, J, Doherty, D

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Novel and recurrent mutations in WISP3 and an atypical phenotype von Bhavani, Gandham SriLakshmi, Shah, Hitesh, Dalal, Ashwin B., Shukla, Anju, Danda, Sumita, Aggarwal, Shagun, Phadke, Shubha R., Gupta, Neerja, Kabra, Madhulika, Gowrishankar, Kalpana, Gupta, Anju, Bhat, Meenakshi, Puri, Ratna D., Bijarnia-Mahay, Sunita, Nampoothiri, Sheela, Mohanasundaram, Kavitha M., Rajeswari, S., Kulkarni, Akhil M., Kulkarni, Muralidhar L., Ranganath, Prajnya, Ramadevi, A. Radha, Hariharan, Sankar V., Girisha, Katta Mohan

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Prenatal detection of deletion-duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversion von Prabhakara, K., Bruno, Damien L., Padman, Priya, Prasad, Suma, Sudheer Kumar, R., Slater, Howard R., Radha Ramadevi, A.

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Premature centromere division versus C-anaphases in cultures: Need for consensus and guidelines von Prabhakara, K., Radha Ramadevi, A.

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Partial 15q22 trisomy due to segregation of maternal 10;15 reciprocal translocation von PRABHAKARA, K, DUTTA, Usha, RADHA RAMADEVI, A

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Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis von DE MUNNIK, Sonja A, BICKNELL, Louise S, HAGEN, Johanna M.van, HENNEKAM, Raoul C, JANSWEIJER, Maaike Ce, JOHNSON, Diana, KANT, Sarina G, OPITZ, John M, RADHA RAMADEVI, A, REARDON, Willie, ROSS, Alison, SARDA, Pierre, AFTIMOS, Salim, SCHRANDER-STUMPEL, Constance Trm, SCHOOTS, Jeroen, KAREN TEMPLE, I, TERHAL, Paulien A, TOUTAIN, Annick, WISE, Carol A, WRIGHT, Michael, SKIDMORE, David L, ESAMUELS, Mark, HHOEFSLOOT, Lies, AL-AAMA, Jumana Y, VAMKNOERS, Nine, BRUNNER, Han G, JACKSON, Andrew P, BONGERS, Ernie Mhf, BEVER, Yolande Van, BOBER, Michael B, CLAYTON-SMITH, Jill, EDREES, Alaa Y, FEINGOLD, Murray, FRYER, Alan

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Meier–Gorlin syndrome: Growth and secondary sexual development of a microcephalic primordial dwarfism disorder von de Munnik, Sonja A., Otten, Barto J., Schoots, Jeroen, Bicknell, Louise S., Aftimos, Salim, Al‐Aama, Jumana Y., van Bever, Yolande, Bober, Michael B., Borm, George F., Clayton‐Smith, Jill, Deal, Cheri L., Edrees, Alaa Y., Feingold, Murray, Fryer, Alan, van Hagen, Johanna M., Hennekam, Raoul C., Jansweijer, Maaike C.E., Johnson, Diana, Kant, Sarina G., Opitz, John M., Ramadevi, A. Radha, Reardon, Willie, Ross, Alison, Sarda, Pierre, Schrander‐Stumpel, Constance T.R.M., Sluiter, A. Erik, Temple, I. Karen, Terhal, Paulien A., Toutain, Annick, Wise, Carol A., Wright, Michael, Skidmore, David L., Samuels, Mark E., Hoefsloot, Lies H., Knoers, Nine V.A.M., Brunner, Han G., Jackson, Andrew P., Bongers, Ernie M.H.F.

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De novo pericentric inversion of chromosome 4, inv(4)(p16q12) in a boy with piebaldism and mental retardation von Ramadevi, A. Radha, Naik, Usha, Dutta, Usha, Srikanth, Prabhakara, K.

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Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18 von Prabhakara, K., Wyandt, Herman E., Huang, Xin L., Prasad, K.Suma, Ramadevi, A.Radha

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Familial (11;21)(p13;q22)pat balanced reciprocal translocation in a female child with regression of milestones von Radha Ramadevi, A., Prabhakara, K., Dutta, Usha

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De novo pericentric inversion of chromosome 4, inv(4)(p16q12) in a boy with piebaldism and mental retardation von Ramadevi, A. Radha, Naik, Usha, Dutta, Usha, Srikanth, Prabhakara, K.

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Prenatal detection of deletion-duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversion von Prabhakara, K, Bruno, Damien L, Padman, Priya, Prasad, Suma, Sudheer Kumar, R, Slater, Howard R, Radha Ramadevi, A

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Meier-Gorlin syndrome: Growth and secondary sexual development of a microcephalic primordial dwarfism disorder von de Munnik, Sonja A., Otten, Barto J., Schoots, Jeroen, Bicknell, Louise S., Aftimos, Salim, Al-Aama, Jumana Y., van Bever, Yolande, Bober, Michael B., Borm, George F., Clayton-Smith, Jill, Deal, Cheri L., Edrees, Alaa Y., Feingold, Murray, Fryer, Alan, van Hagen, Johanna M., Hennekam, Raoul C., Jansweijer, Maaike C.E., Johnson, Diana, Kant, Sarina G., Opitz, John M., Ramadevi, A. Radha, Reardon, Willie, Ross, Alison, Sarda, Pierre, Schrander-Stumpel, Constance T.R.M., Sluiter, A. Erik, Temple, I. Karen, Terhal, Paulien A., Toutain, Annick, Wise, Carol A., Wright, Michael, Skidmore, David L., Samuels, Mark E., Hoefsloot, Lies H., Knoers, Nine V.A.M., Brunner, Han G., Jackson, Andrew P., Bongers, Ernie M.H.F.

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Revolutionizing cancer treatment: ROS-induced apoptosis via nanoformulated alkaloids von Putta, Swathi, Chinnaiyan, Santhosh Kumar, Korni, Ramadevi, Gadela, Venkata Radha

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Mutational Analysis of Androgen Receptor Gene in Two Families with Androgen Insensitivity von Akella, Radha Ramadevi

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Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation von Sheth, Jayesh, Bhavsar, Riddhi, Mistri, Mehul, Pancholi, Dhairya, Bavdekar, Ashish, Dalal, Ashwin, Ranganath, Prajnya, Girisha, Katta M, Shukla, Anju, Phadke, Shubha, Puri, Ratna, Panigrahi, Inusha, Kaur, Anupriya, Muranjan, Mamta, Goyal, Manisha, Ramadevi, Radha, Shah, Raju, Nampoothiri, Sheela, Danda, Sumita, Datar, Chaitanya, Kapoor, Seema, Bhatwadekar, Seema, Sheth, Frenny

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Maternal cardiac function in gestational hypertension, mild and severe preeclampsia and normal pregnancy: A comparative study von Tatapudi, Radha, Pasumarthy, L. Ramadevi

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Congenital Disorder of Glycosylation (CDG) Presenting as Non-immune Hydrops Fetalis von Panigrahy, Nalinikanta, Lingappa, Lokesh, Ramadevi, Akela Radha, Venkatlakshmi, Alla

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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

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Preparation, characterization, and conductivity of YLnTiZrO7 (Ln = La, Nd, Sm, and Eu) von V., Ramadevi, G., Ravi, Velchuri, Radha, C. H., Sameera Devi, G., Prasad, M., Vithal

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