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Search Results - Parameswaran, Arun Sree
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Kernicterus caused by a rare genetic variant of Crigler-Najjar Syndrome (c.826G>C)
by
Agarwal, Saurabh
,
UK, Kandha Kumar
,
Parameswaran, Arun Sree
,
Saini, Lokesh
,
Singh, Kuldeep
Published in
Indian journal of pediatrics
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Chromosome Xp22.3 deletion syndrome with X-linked ichthyosis, Kallmann syndrome, short stature, generalized epilepsy, hearing loss, attention deficit hyperactivity disorder, and in...
by
Gunasekaran, Pradeep Kumar
,
Saini, Lokesh
,
Rajial, Tanuja
,
Manjunathan, Sujatha
,
Laxmi, Veena
,
Gupta, Rahul
,
Kumar, Ashna
,
Parameswaran, Arun Sree
,
Palayullakandi, Achanya
,
Budania, Anil
,
Singh, Kuldeep
Published in
Journal of neurosciences in rural practice
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Indian Journal Of Pediatrics
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