Proband only exome sequencing in 403 Indian children with neurodevelopmental disorders: Diagnostic yield, utility and challenges in a resource-limited setting von Pranav Chand, Rayabarapu, Vinit, Wankhede, Vaidya, Varsha, Iyer, Anand Subramaniam, Shelke, Madhavi, Aggarwal, Shagun, Magar, Suvarna, Danda, Sumita, Moirangthem, Amita, Phadke, Shubha Rajendra, Goyal, Manisha, Ranganath, Prajnya, Mistri, Mehul, Shah, Parth, Shah, Nidhi, Kotecha, Udhaya Hardik

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Adrenoleukodystrophy: The Importance of Early MRI Findings and Serial Imaging von Jain, Neeraj, Phadke, Rajendra, Phadke, Shubha, Dwivedi, Aradhana

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Hemiconvulsion-hemiplegia-epilepsy syndrome with 1q44 microdeletion: Causal or chance association von Gupta, Rekha, Agarwal, Meenal, Boqqula, Vijay R., Phadke, Rajendra V., Phadke, Shubha R.

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Red cell alloimmunization and associated risk factors in multiply transfused thalassemia patients: A prospective cohort study conducted at a tertiary care center in Northern India von Yadav, Brijesh Kumar, Chaudhary, Rajendra K, Elhence, Priti, Phadke, Shubha Rao, Mandal, Kausik, Saxena, Deepti, Moirangthem, Amita

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A new autosomal recessive disorder of bilateral frontotemporal pachygyria without microcephaly: report of a case and review of literature von Phadke, Shubha R, Girisha, K M, Phadke, Rajendra V

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Severe form of congenital cerebral and cerebellar atrophy: A neurodegenerative disorder of fetal onset von Phadke, Shubha, Puri, Ratna, Phadke, Rajendra

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Absence of HTLV‐1 infection in multi‐transfused thalassemia patients in North India von Chaudhary, Rajendra, Phadke, Shubha R.

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Severe form of congenital cerebral and cerebellar atrophy: A neurodegenerative disorder of fetal onset von Phadke, Shubha, Puri, Ratna, Phadke, Rajendra

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