Pediatric Endocrine Disorders Fourth Edition Meena P Desai, PSN Menon, ViJAYALAKSHMI BhATIA, Anju Seth: Orient BlackSwan Pvt. Ltd, Pages: 584; Price: Rs. 1,895 von Dayal, Devi

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

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

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

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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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Aldosteronoma in childhood: A review of clinical features and management von Agarwala, S., Mitra, D.K., Bhatnagar, V., Menon, P.S.N., Gupta, A.K.

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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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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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Pediatric Endocrine DisordersFourth EditionMeena P Desai, PSN Menon, ViJAYALAKSHMI BhATIA, Anju Seth: Orient BlackSwan Pvt. Ltd, Pages: 584; Price: Rs. 1,895 von Dayal, Devi

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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 MR, Prahlad B, Kumar V, Mathur R, Hamilton S, Kabra M, Menon PSN, Verma IC

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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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MP Desai B Bhatia Paedialric Endocrine Disorders 2001 PSN Menon Orient Longman Chennai 440 Price Rs.425.00 von Nair, MNG

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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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