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Congenital Anemia

Clinical, genetic and cytogenetic study of Fanconi anemia in an Indian population

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Pages 58-62 | Published online: 18 Jul 2013

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Atreyee Dutta, Rajib De, Tuphan Kanti Dolai, Pritha Pal, Shanoli Ghosh, Pradip Kumar Mitra & Ajanta Halder. (2018) Incidence of Fanconi anaemia in phenotypically normal aplastic anaemia patients in West Bengal. Hematology 23:7, pages 405-412.
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Sunil Kumar Polipalli, Ankur Jindal, Madhavi Puppala & Seema Kapoor. (2023) Cytogenetic analysis of fanconi anemia patients: An hospital based study. International Journal of Clinical Biochemistry and Research 10:3, pages 204-209.
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Colette B. Rogers, Rachel E. Kram, Kevin Lin, Chad L. Myers, Alexandra Sobeck, Eric A. Hendrickson & Anja-Katrin Bielinsky. (2023) Fanconi anemia-associated chromosomal radial formation is dependent on POLθ-mediated alternative end joining. Cell Reports 42:5, pages 112428.
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Anjali Shah, Merin George, Somprakash Dhangar, Aruna Rajendran, Sheila Mohan & Babu Rao Vundinti. (2021) Severe telomere shortening in Fanconi anemia complementation group L. Molecular Biology Reports 48:1, pages 585-593.
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Fakeha Siddiqui, Saqib Ansari, Akbar Agha, Nadeem Nusrat, Saima Munzir, Saira Shan, Anny Hanifa, Tasneem Farzana, Mehwesh Taj, Munira Borhany, Zeeshan Hussain, Muhammad Nadeem & Tahir Shamsi. (2020) Chromosomal Breakage in Fanconi Anemia and Consanguineous Marriages: A Social Dilemma for Developing Countries. Cureus.
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Michael A. Petr, Tulika Tulika, Lina M. Carmona-Marin & Morten Scheibye-Knudsen. (2020) Protecting the Aging Genome. Trends in Cell Biology 30:2, pages 117-132.
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Fathelrahman Elawad Ahmed. (2016) Fanconi’s Anemia among Sudanese Children: A Report of Forty Cases. Hematology & Transfusion International Journal 3:3.
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Ponnumony John Solomon, Priya Margaret, Ramya Rajendran, Revathy Ramalingam, Godfred A Menezes, Alph S Shirley, Seung Jun Lee, Moon-Woo Seong, Sung Sup Park, Dodam Seol & Soo Hyun Seo. (2015) A case report and literature review of Fanconi Anemia (FA) diagnosed by genetic testing. Italian Journal of Pediatrics 41:1.
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Pavithra Shyamsunder, Kripa S. Ganesh, Prasanna Vidyasekar, Sheila Mohan & Rama Shanker Verma. (2013) Identification of novel target genes involved in Indian Fanconi anemia patients using microarray. Gene 531:2, pages 444-450.
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Faten Talmoudi, Lobna Kammoun, Nizar Benhalim, Lamia Torjemane, Monia Ouederni, Lamia Aissaoui, Amel Lakhal, Fethi Mellouli, Tarek B. Othmen, Mohamed Bejaoui, Sonia Abdelhak, Mounira Meddeb, Koussay Dellagi, Sondes Hdiji & Ahlem Amouri. (2013) Cytogenetic Assessment of Fanconi Anemia in Children With Aplastic Anemia in Tunisia. Journal of Pediatric Hematology/Oncology 35:7, pages 547-550.
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Dharmendra Jain, Ritesh Kumar, Neetu Tyagi, Avinash Negi, Amit Pande, Amita Mahajan, Prashant K. Pandey, Radhika Malik, Vimarsh Raina & Balwant K. Malik. (2012) Etiology and Survival of Aplastic Anemia: A Study Based on Clinical Investigation. Journal of Clinical Laboratory Analysis 26:6, pages 452-458.
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Dharmendra Jain, Ritesh Kumar, Balwant Kishan Malik & Vimarsh Raina. (2012) Copy neutral LOH of FANC F gene: implication on differential diagnosis and treatment of aplastic anemia: letter. European Journal of Haematology 89:4, pages 365-366.
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Paulo Ricardo G Zen, Felipe Nora de Moraes, Rafael Fabiano M Rosa, Carla Graziadio & Giorgio Adriano Paskulin. (2011) Características clínicas de pacientes com anemia de Fanconi. Revista Paulista de Pediatria 29:3, pages 392-399.
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Philip S. Rosenberg, Hannah Tamary & Blanche P. Alter. (2011) How high are carrier frequencies of rare recessive syndromes? Contemporary estimates for Fanconi Anemia in the United States and Israel. American Journal of Medical Genetics Part A 155:8, pages 1877-1883.
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