टीमोठी सिंड्रोम (Hindi Wikipedia)

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Marks M, Whisler S, Clericuzio C, Keating M (1995). "A new form of long QT syndrome associated with syndactyly". J Am Coll Cardiol. 25 (1): 59–64. PMID 7798527. डीओआइ:10.1016/0735-1097(94)00318-K.सीएस1 रखरखाव: एक से अधिक नाम: authors list (link)
Marks M, Trippel D, Keating M (1995). "Long QT syndrome associated with syndactyly identified in females". Am J Cardiol. 76 (10): 744–5. PMID 7572644. डीओआइ:10.1016/S0002-9149(99)80216-1.सीएस1 रखरखाव: एक से अधिक नाम: authors list (link)

Marks M, Whisler S, Clericuzio C, Keating M (1995). "A new form of long QT syndrome associated with syndactyly". J Am Coll Cardiol. 25 (1): 59–64. PMID 7798527. डीओआइ:10.1016/0735-1097(94)00318-K.सीएस1 रखरखाव: एक से अधिक नाम: authors list (link)
Marks M, Trippel D, Keating M (1995). "Long QT syndrome associated with syndactyly identified in females". Am J Cardiol. 76 (10): 744–5. PMID 7572644. डीओआइ:10.1016/S0002-9149(99)80216-1.सीएस1 रखरखाव: एक से अधिक नाम: authors list (link)
Splawski I, Timothy K, Sharpe L, Decher N, Kumar P, Bloise R, Napolitano C, Schwartz P, Joseph R, Condouris K, Tager-Flusberg H, Priori S, Sanguinetti M, Keating M (2004). "Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism". Cell. 119 (1): 19–31. PMID 15454078. डीओआइ:10.1016/j.cell.2004.09.011.सीएस1 रखरखाव: एक से अधिक नाम: authors list (link)
Splawski I, Timothy K, Decher N, Kumar P, Sachse F, Beggs A, Sanguinetti M, Keating M (2005). "Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations". Proc Natl Acad Sci USA. 102 (23): 8089–96, discussion 8086–8. PMID 15863612. डीओआइ:10.1073/pnas.0502506102. पी॰एम॰सी॰ 1149428.सीएस1 रखरखाव: एक से अधिक नाम: authors list (link)

Marks M, Whisler S, Clericuzio C, Keating M (1995). "A new form of long QT syndrome associated with syndactyly". J Am Coll Cardiol. 25 (1): 59–64. PMID 7798527. डीओआइ:10.1016/0735-1097(94)00318-K.सीएस1 रखरखाव: एक से अधिक नाम: authors list (link)
Marks M, Trippel D, Keating M (1995). "Long QT syndrome associated with syndactyly identified in females". Am J Cardiol. 76 (10): 744–5. PMID 7572644. डीओआइ:10.1016/S0002-9149(99)80216-1.सीएस1 रखरखाव: एक से अधिक नाम: authors list (link)
Splawski I, Timothy K, Sharpe L, Decher N, Kumar P, Bloise R, Napolitano C, Schwartz P, Joseph R, Condouris K, Tager-Flusberg H, Priori S, Sanguinetti M, Keating M (2004). "Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism". Cell. 119 (1): 19–31. PMID 15454078. डीओआइ:10.1016/j.cell.2004.09.011.सीएस1 रखरखाव: एक से अधिक नाम: authors list (link)
Splawski I, Timothy K, Decher N, Kumar P, Sachse F, Beggs A, Sanguinetti M, Keating M (2005). "Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations". Proc Natl Acad Sci USA. 102 (23): 8089–96, discussion 8086–8. PMID 15863612. डीओआइ:10.1073/pnas.0502506102. पी॰एम॰सी॰ 1149428.सीएस1 रखरखाव: एक से अधिक नाम: authors list (link)

Splawski I, Timothy K, Decher N, Kumar P, Sachse F, Beggs A, Sanguinetti M, Keating M (2005). "Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations". Proc Natl Acad Sci USA. 102 (23): 8089–96, discussion 8086–8. PMID 15863612. डीओआइ:10.1073/pnas.0502506102. पी॰एम॰सी॰ 1149428.सीएस1 रखरखाव: एक से अधिक नाम: authors list (link)