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Research Articles

Heterochromatin extension: a possible cytogenetic fate of primary amenorrhea along with normal karyotype

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References

  • Agacayak E, Icen MS, Tunc SY, Siddik Evsen M, Kalkanli S, Basaranoglu S. 2014. The frequency and the type of different etiological factors in primary amenorrhea. Acta Medica Mediterranea 30:383–387.
  • An C, Tang D, Wu M, Ding X, Jiang X. 2016. Major chromosomal abnormalities and chromosome polymorphism in 1543 couples with recurrent miscarriages in Hubei province of China. Biomedical Research 27:1395–1401.
  • Bannister AJ, Kouzarides T. 2011. Regulation of chromatin by histone modifications. Cell Research 21:381–395.
  • Bhuyan AK, Sarma D, Saikia UK. 2012. Contemporary issues in primary amenorrhea: an experience from a Tertiary Care Center. Indian Journal of Endocrinology and Metabolism 16:387–388.
  • Dutta UR, Ponnala R, Pidugu VK, Dalal AB. 2013. Chromosomal abnormalities in amenorrhea: a retrospective study and review of 637 patients in South India. Archives of Iranian Medicine 16:267–270.
  • El-Dahtory F. 2012. Chromosomal abnormalities and hormonal disorders of primary amenorrhea patients in Egypt. Indian Journal of Human Genetics 18:183–186.
  • Freed D, Aldana R, Weber JA, Edwards JS. 2017. The Sentieon Genomics Tools – a fast and accurate solution to variant calling from next-generation sequence data. BioRxiv.
  • Ghosh S, Roy S, Pal P, Dutta A, Halder A. 2018. Cytogenetic analysis of patients with primary amenorrhea in Eastern India. Journal of Obstetrics and Gynaecology 38:270–276.
  • Kalavathi V, Chandra N, Renjini Nambiar G, Shanker J, Sugunashankari P, Meena J, et al. 2010. Chromosomal abnormalities in 979 cases of amenorrhea: a review. International Journal of Human Genetics 10:65–69.
  • Malla TM, Dar FA, Pandith AA, Zargar MH. 2016. Frequency and pattern of cytogenetic alterations in primary amenorrhea cases of Kashmir, North India. Egyptian Journal of Medical Human Genetics 17:25–31.
  • McLaren W, Pritchard B, Rios D, Chen Y, Flicek P, Cunningham F. 2010. Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor. Bioinformatics 26:2069–2070.
  • Safaei A, Vasei M, Ayatollahi H. 2010. Cytogenetic analysis of patients with primary amenorrhea in Southwest of Iran. Iranian Journal of Pathology 5:121–125.
  • Tempest HG, Simpson JL. 2017. Why are we still talking about chromosomal heteromorphisms? Reproductive Biomedicine Online 35:1–2.
  • Vijayalakshmi J, Koshy T, Kaur H, Andrea Mary F, Selvi R, Deepa Parvathi V, et al. 2010. Cytogenetic analysis of patients with primary amenorrhea. International Journal of Human Genetics 10:71–76.
  • Zerbino DR, Achuthan P, Akanni W, Amode MR, Barrell D, Bhai J, et al. 2018. Ensembl 2018. Nucleic Acids Research 46:D754–D761.

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