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Journal of Obstetrics and Gynaecology Volume 38, 2018 - Issue 2
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Original Article

Cytogenetic analysis of patients with primary amenorrhea in Eastern India

Shaulee Ghosha Department of Genetics, Vivekananda Institute of Medical Sciences, Kolkata, India; Correspondence[email protected]
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,
Sanchita Royb Department of Anatomy, Institute of Post–Graduation Medical Education and Research, Kolkata, IndiaView further author information
,
Pritha Pala Department of Genetics, Vivekananda Institute of Medical Sciences, Kolkata, India; View further author information
,
Atreyee Duttaa Department of Genetics, Vivekananda Institute of Medical Sciences, Kolkata, India; View further author information
&
Ajanta Haldera Department of Genetics, Vivekananda Institute of Medical Sciences, Kolkata, India; View further author information
Pages 270-275 | Received 23 Aug 2016, Accepted 07 Jun 2017, Published online: 12 Oct 2017

Citations (8)

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Read on this site (2)

Bishal Kumar Dey, Shanoli Ghosh, Ajanta Halder, Somajita Chakraborty & Sanchita Roy. (2022) Heterochromatin extension: a possible cytogenetic fate of primary amenorrhea along with normal karyotype. Journal of Obstetrics and Gynaecology 42:6, pages 2314-2319.
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B. Chen, L. Li, J. Wang, Y. Zhou, J. Zhu, T. Li, H. Pan, B. Liu, Y. Cao & B. Wang. (2018) Identification of the first homozygous POLG mutation causing non-syndromic ovarian dysfunction. Climacteric 21:5, pages 467-471.
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Articles from other publishers (6)

Christy Vijay, S Amudha, Preetha Tilak, Mary Margaret & P Raina. (2024) Cytogenetic Abnormalities Identified in Cases of Amenorrhea. Journal of South Asian Federation of Obstetrics and Gynaecology 16:1, pages 6-11.
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Divya Chandel, Priyanka Sanghavi & Ramtej Verma. (2023) Clinical profile and cytogenetic correlations in females with primary amenorrhea. Clinical and Experimental Reproductive Medicine 50:3, pages 192-199.
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Bushra A. Kanaan, Mushtak T.S. Al-Ouqaili & Rafal M. Murshid. (2023) Cytogenetic screening of chromosomal abnormalities and genetic analysis of FSH receptor Ala307Thr and Ser680Asn genes in amenorrheic patients. PeerJ 11, pages e15267.
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Vinayak Kulkarni, Selvaa Kumar Chellasamy, Somprakash Dhangar, Jagdeeshwar Ghatanatti & Babu Rao Vundinti. (2023) Comprehensive molecular analysis identifies eight novel variants in XY females with disorders of sex development. Molecular Human Reproduction 29:2.
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Sriambika Kumar & Rema Devi. (2022) Clinical spectrum and Cytogenetic characterization of patients with Turner Syndrome – Twin case report. Journal of Current Research in Scientific Medicine 8:2, pages 192.
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Shanoli Ghosh, Sanchita Roy & Ajanta Halder. (2020) Study of frequency and types of chromosomal abnormalities in phenotypically female patients with amenorrhea in Eastern Indian population. Journal of Obstetrics and Gynaecology Research 46:9, pages 1627-1638.
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