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Search Results - Bari, Shreya
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Genetic testing and family screening in idiopathic pediatric cardiomyopathy: a prospective observational study from a tertiary care center in North India
by
Bhatt, Dheeraj D
,
Mathews, Susi
,
Ahuja, Vanshika
,
Shamim, Uzma
,
Uppilli, Bharathram
,
Bari, Shreya
,
Kumar, Dinesh
Published in
The Egyptian journal of medical human genetics
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Spinocerebellar ataxia type 27B (SCA27B) in India: insights from a large cohort study suggest ancient origin
by
De, Tiyasha
,
Sharma, Pooja
,
Upilli, Bharathram
,
Vivekanand, A.
,
Bari, Shreya
,
Sonakar, Akhilesh Kumar
,
Srivastava, Achal Kumar
,
Faruq, Mohammed
Published in
Neurogenetics
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Genetics of 67 patients of suspected primary ciliary dyskinesia from India
by
Jat, Kana Ram
,
Faruq, Mohammed
,
Jindal, Shishir
,
Bari, Shreya
,
Soni, Akshita
,
Sharma, Pooja
,
Mathews, Susi
,
Shamim, Uzma
,
Ahuja, Vanshika
,
Uppilli, Bharathram
,
Yadav, Subhash C.
,
Lodha, Rakesh
,
Arava, Sudheer K.
,
Kabra, Sushil K.
Published in
Clinical genetics
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Novel PANK2 Variant in Asian Indians with Atypical Pantothenate Kinase Associated Neurodegeneration
by
Saini, Arti
,
Holla, Vikram V.
,
Kalikavil Puthanveedu, Divya
,
Mehta, Sahil
,
Elavarasi, Arunmozhimaran
,
Pillai, Kanchana Soman
,
Mohapatra, Prachi
,
Kumari, Riyanka
,
Bari, Shreya
,
Singh, Inder
,
Cherian, Ajith
,
Krishnan, Syam
,
Radhakrishnan, Divya M.
,
Agarwal, Ayush
,
Garg, Divyani
,
Garg, Kanwaljeet
,
Singh, Manmohan
,
Garg, Ajay
,
Muthusamy, Babylakshmi
,
Lal, Vivek
,
Kishore, Asha
,
Pal, Pramod Kumar
,
Srivastava, Achal
,
Faruq, Mohammed
,
Rajan, Roopa
Published in
Movement disorders
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Egyptian Journal Of Medical Human Genetics
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