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The Journal of Maternal-Fetal & Neonatal Medicine Volume 24, 2011 - Issue 1
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Genotyping of the C742T mutation of the FGFR3 gene causing type 1 thanatophoric dysplasia by high-resolution melting analysis

Ying-Na LiuPrenatal Diagnostic Center, Guangzhou Maternal and Neonatal Hospital, Guangzhou Women and Children's Medical Center, Guangzhou Medical College, Guangzhou, Guangdong, China
,
Ru LiPrenatal Diagnostic Center, Guangzhou Maternal and Neonatal Hospital, Guangzhou Women and Children's Medical Center, Guangzhou Medical College, Guangzhou, Guangdong, China
&
Dong-Zhi LiPrenatal Diagnostic Center, Guangzhou Maternal and Neonatal Hospital, Guangzhou Women and Children's Medical Center, Guangzhou Medical College, Guangzhou, Guangdong, ChinaCorrespondence[email protected]
Pages 186-188 | Received 07 Feb 2010, Accepted 08 Mar 2010, Published online: 23 Jun 2010

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L. Zhen, M. Pan, J. Han, X. Yang, C. Liao & D. Z. Li. (2015) Increased first-trimester nuchal translucency associated with thanatophoric dysplasia type 1. Journal of Obstetrics and Gynaecology 35:7, pages 685-687.
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Yu Yang, Ying-Na Liu & Dong-Zhi Li. (2012) Rapid Detection of Common Mutations of the FGFR3 Gene Causing Thanatophoric Dysplasia Type I: Two Case Reports. Fetal and Pediatric Pathology 31:3, pages 128-133.
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Articles from other publishers (2)

Fernanda Rolemberg G. Riba, Maria E.S. GomesNatana Chaves RabeloMaria Celia C. ZumaJuan C. LlerenaAndré Luiz MencalhaSayonara Gonzalez. (2021) High-Resolution Melting Analysis for Rapid Detection of Mutations in Patients with FGFR3 -Related Skeletal Dysplasias . Genetic Testing and Molecular Biomarkers 25:10, pages 674-682.
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Guanglin Cui, Lina Zhang, Yujun Xu, Katherine Cianflone, Hu Ding & Dao Wen Wang. (2013) Development of a high resolution melting method for genotyping of risk HLA-DQA1 and PLA2R1 alleles and ethnic distribution of these risk alleles. Gene 514:2, pages 125-130.
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