Contemporary issues in precocious puberty von Bajpai, Anurag, Menon, P S N

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Dominant and recessive deafness caused by mutations of a novel gene, TMC1 , required for cochlear hair-cell function von Griffith, Andrew J, Kurima, Kiyoto, Peters, Linda M, Yang, Yandan, Riazuddin, Saima, Ahmed, Zubair M, Naz, Sadaf, Arnaud, Deidre, Drury, Stacy, Mo, Jianhong, Makishima, Tomoko, Ghosh, Manju, Menon, P.S.N, Deshmukh, Dilip, Oddoux, Carole, Ostrer, Harry, Khan, Shaheen, Riazuddin, Sheikh, Deininger, Prescott L, Hampton, Lori L, Sullivan, Susan L, Battey, James F, Keats, Bronya J.B, Wilcox, Edward R, Friedman, Thomas B

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Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC von AHMED, Zubair M, SMITH, Tenesha N, FRIEDMAN, Thomas B, WILCOX, Edward R, RIAZUDDIN, Saima, MAKISHIMA, Tomoko, GHOSH, Manju, BOKHARI, Sirosh, MENON, Puthezhath S. N, DESHMUKH, Dilip, GRIFFITH, Andrew J, RIAZUDDIN, Sheikh

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Editorials von Menon, PSN, Gaur, Ajay, Bhattacharya, Sujit K, Sur, Dipika, Mahalanabis, Dilip

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Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome von LIBURD, Nikki, GHOSH, Manju, SMITH, Ann C. M, CHEN, Ken-Shiung, LUPSKI, James R, WILCOX, Edward R, POTOCKI, Lorraine, FRIEDMAN, Thomas B, RIAZUDDIN, Saima, NAZ, Sadaf, KHAN, Shaheen, AHMED, Zubair, RIAZUDDIN, Sheikh, YONG LIANG, MENON, Puthezhath S. N, SMITH, Tenesha

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Editorials von Menon, PSN, Gaur, Ajay, Bhattacharya, Sujit K, Sur, Dipika, Mahalanabis, Dilip

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Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario von Maheshwari, Manjula, Vijaya, R., Ghosh, Manju, Shastri, Shivaram, Kabra, Madhulika, Menon, P.S.N.

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HLA haplotypes associated with type 1 diabetes mellitus in north indian children von Kanga, Uma, Vaidyanathan, Balu, Jaini, Ritika, Menon, Puthezath S.N, Mehra, Narinder K

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Cytogenetic causes for recurrent spontaneous abortions - An experience of 742 couples (1484 cases) von Dubey, S, Chowdhury, M, Prahlad, B, Kumar, V, Mathur, R, Hamilton, S, Kabra, M, Menon, P, Verma, I

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Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism: Indian experience von CHOWDHURY, M. R, TIWARI, M, KABRA, M, MENNN, P. S. N

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Hypothalamic hamartoma, gelastic epilepsy, precocious puberty – a diffuse cerebral dysgenesis von Gulati, Sheffali, Gera, Sameer, Menon, P.S.N, Kabra, Madhulika, Kalra, Veena

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Factor IX gene polymorphisms in Indian population von Chowdhury, Madhumita Roy, Kabra, Madhulika, Menon, P.S.N.

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Detection of complex chromosomal rearrangements in a woman with repeated spontaneous abortions von DUBEY, Sudhisha, MATHUR, Roli, KABRA, Madhulika, MENON, Puthezhath S. N

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Factor VIII gene polymorphisms in the Asian Indian population von Chowdhury, M. R., Herrmann, F. H., Schroder, W., Lambert, C. T., Lalloz, M. R. A., Layton, M., Kumbnani, H. K., Kabra, M., Menon, P. S. N., Verma, I. C.

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Cytogenetic causes for recurrent spontaneous abortions - An experience of 742 couples (1484 cases) von Dubey S, Chowdhury MR, Prahlad B, Kumar V, Mathur R, Hamilton S, Kabra M, Menon PSN, Verma IC

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Diagnosis and management of congenital adrenal hyperplasia: clinical, molecular and prenatal aspects von Mathur, R, Kabra, M, Menon, P S

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The challenge of haemoglobinopathies in India von Kabra, M, Menon, P S

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Rapid prenatal karyotyping using foetal blood obtained by cordocentesis von Mathur, Roli, Dubey, Sudhisha, Hamilton, Shireen, Singh, Geeta, Deka, Deepika, Kriplani, Alka, Kabra, Madhulika, Menon, P S N

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Hypothalamic hamartoma : Report of a case with unusual histologic features von SHARMA, M. C, GAIKWAD, S, MAHAPATRA, A. K, MENON, P. S. N, SARKAR, C

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Prenatal diagnosis of haemoglobinopathies von Arora, S, Kabra, M, Maheshwari, M, Shastri, S, Kaur, D, Deka, D, Kriplani, A, Menon, P S

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