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Whole exome sequencing uncovered highly penetrant recessive mutations for a spectrum of rare genetic pediatric diseases in Bangladesh |
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| Hosneara Akter, Mohammad Shahnoor Hossain, Nushrat Jahan Dity, Md. Atikur Rahaman, K. M. Furkan Uddin, Nasna Nassir, Ghausia Begum, Reem Abdel Hameid, Muhammad Sougatul Islam, Tahrima Arman Tusty, Mohammad Basiruzzaman, Shaoli Sarkar, Mazharul Islam, Sharmin Jahan, Elaine T. Lim, Marc Woodbury-Smith, Dimitri James Stavropoulos, Darren D. O’Rielly, Bakhrom K. Berdeiv, A. H. M. Nurun Nabi, Mohammed Nazmul Ahsan, Stephen W. Scherer, Mohammed Uddin |
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| npj Genomic Medicine. 2021; 6(1) |
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2 |
Bardet-Biedl Syndrome with Urogenital Sinus Presenting with Acute Renal Failure in a Neonate |
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| Nandini K. Bedi,Dhruv Grover |
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| The Indian Journal of Pediatrics. 2013; |
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3 |
Bardet–Biedl Syndrome: A Rare Cause of Chronic Kidney Disease |
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| Indian Journal of Clinical Biochemistry. 2013; 28(2): 201 |
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Bardet–Biedl syndrome presenting as dilated cardiomyopathy |
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| D.J.K. Chakravarthy,Y.S. Sarma,M. Sriharibabu,K. Subhramanyam,T. Sivakumar,K. Chandrakanth |
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| Journal of Indian College of Cardiology. 2013; |
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End Stage Renal Disease, Differential Diagnosis, A Rare Genetic Disorder: Bardet–Biedl Syndrome: Case Report and Review |
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| B. Sowjanya, U. Sreenivasulu, J. N. Naidu, N. Sivaranjani |
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| Indian Journal of Clinical Biochemistry. 2011; |
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Bardet-Biedl syndrome with end-stage kidney disease in a four-year-old Romanian boy: a case report |
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| Cristina M Mihai, Jan D Marshall, Ramona M Stoicescu |
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| Journal of Medical Case Reports. 2011; 5(1): 378 |
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7 |
Continuous Ambulatory Peritoneal Dialysis for a Patient With Bardet-Biedl Syndrome |
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| Momtaz, H.E. and Amanati, A. |
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| Iranian Journal of Kidney Diseases. 2008; 2(4) |
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