Author:
Biswas Pronama,Verma Rama Shankar
Publisher
Springer Science and Business Media LLC
Reference88 articles.
1. Alter, B. P., Baerlocher, G. M., Savage, S. A., Chanock, S. J., Weksler, B. B., Willner, J. P., Peters, J. A., Giri, N., & Lansdorp, P. M. (2007). Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita. Blood, 110(5), 1439–1447. https://doi.org/10.1182/blood-2007-02-075598
2. Asur, R. S., Kimble, D. C., Lach, F. P., Jung, M., Donovan, F. X., Kamat, A., Noonan, R. J., Thomas, J. W., Park, M., Chines, P., Vlachos, A., Auerbach, A. D., Smogorzewska, A., & Chandrasekharappa, S. C. (2018). Somatic mosaicism of an intragenic FANCB duplication in both fibroblast and peripheral blood cells observed in a Fanconi anemia patient leads to milder phenotype. Molecular Genetics and Genomic Medicine, 6(1), 77–91. https://doi.org/10.1002/mgg3.350
3. Auerbach, A. D., Adler, B., & Chaganti, R. S. K. (1981). Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method. Pediatrics, 67(1), 128–135.
4. Ballif, B. C., Rorem, E. A., Sundin, K., Lincicum, M., Gaskin, S., Coppinger, J., Kashork, C. D., Shaffer, L. G., & Bejjani, B. A. (2006). Detection of low-level mosaicism by array CGH in routine diagnostic specimens. American Journal of Medical Genetics. Part A, 140(24), 2757–2767. https://doi.org/10.1002/ajmg.a.31539
5. Ballmaier, M., & Germeshausen, M. (2011). Congenital amegakaryocytic thrombocytopenia: Clinical presentation, diagnosis, and treatment. Seminars in Thrombosis and Hemostasis, 37(6), 673–681. https://doi.org/10.1055/s-0031-1291377