Cytogenetic Analysis in Cases with Sex Anomalies
Author:
Affiliation:
1. Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar, 143005, Punjab, India
Publisher
Kamla Raj Enterprises
Subject
Genetics (clinical),Genetics
Link
https://www.tandfonline.com/doi/pdf/10.1080/09723757.2004.11885887
Reference6 articles.
1. Gravholt CH, Fedder J, Naeraa RW and Muller J 2000. Occurrence of gonadoblastoma in females with Turner syndrome and Y chromosome material: A population study. JClin Endocrin Metabol,85 (9): 3199–3202.
2. Kaur R, Gandhi G, Singh JR 1996. Cytogenetic studies in referred cases-an Indian experience. In: JR Singh (Ed.)Current Concepts in Human Genetics, Amritsar: GND University Press, pp: 97-101.
3. Mancilla EE, Poggi H, Repetto G, Rumie H, Garcia H, Ugarte F, Hidalgo S, Jara A, Muzzo S, Panteon E, Torrealba I, Foradori A, Cattani A 2003. Y chromosome sequences in Turner’s syndrome: association with virilization and gonadoblastoma.J Pediat Endocrinol Metab,16 (8): 1157–1163.
4. Okten G, Elbystan M, Kokcu A, Kara N, Bagci H 1998. Genotype and X chromatin percentages of genital organ anomalies in areas of Samsun Turkey. In: JR Singh, K Sperling, M Neitzal (eds.)Progress in Human Genetics. Amritsar: GND University Press, pp: 244-259.
5. Queipo G, Zenteno JC, Pena R, Nieto K, Radillo A, Dorantes LM, Erana L, Lieberman E, Soderlund D, Jimenez AL, Ramon G, Kofman-Alfaro S 2002. Molecular analysis in true hermaphroditism: demonstration of low level hidden mosaicism for Y-derived sequences in 46,XX cases.Hum Genet,111(3): 278–283.
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