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The Journal of Maternal-Fetal & Neonatal Medicine Volume 22, 2009 - Issue 12
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Case Reports

A case of 48,XXYY syndrome detected prenatally by QF-PCR

Qiu-Shi ZhangPrenatal Diagnostic Center, Guangzhou Maternal and Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, China
&
Dong-Zhi LiPrenatal Diagnostic Center, Guangzhou Maternal and Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, ChinaCorrespondence[email protected]
Pages 1214-1216 | Received 18 Nov 2008, Accepted 07 May 2009, Published online: 16 Nov 2009

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Jian Li, Li Zhen, Min Pan & Dong-Zhi Li. (2020) First prenatal case of 48,XXYY syndrome detected by maternal cell-free DNA testing. Journal of Obstetrics and Gynaecology 40:2, pages 270-272.
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Articles from other publishers (2)

Aránzazu Margallo Balsera, Manuela Núñez Estévez, Emilia Balboa Beltrán, Plácida Sánchez-Giralt, Luz González García, Trinidad Herrera Moreno, Mayte García de Cáceres, José M Carbonell Pérez, Enrique Galán Gómez & Raquel Rodríguez-López. (2013) Distinct mechanism of formation of the 48, XXYY karyotype. Molecular Cytogenetics 6:1.
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S. Kemeny, C. Pebrel-Richard, L. Gouas, L. Veronese, D. Lemery, A. Tchirkov, C. Goumy & P. Vago. (2013) Prenatal ultrasound diagnosis of a 48,XXYY syndrome. Morphologie 97:317, pages 65-67.
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