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Hemoglobin
international journal for hemoglobin research
Volume 25, 2001 - Issue 1
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Original

PRENATAL DIAGNOSIS OF β-THALASSEMIA MAJOR BY HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY ANALYSIS OF HEMOGLOBINS IN FETAL BLOOD SAMPLES

Torpong Sanguansermsri Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang MaiThailand; Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai50200, Thailand
,
Patra Thanarattanakorn Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang MaiThailand
,
Heinrich F. Steger Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang MaiThailand
,
Theera Tongsong Department of Obstetrics and Gynecology, Faculty of Medicine, Chiang Mai University, Chiang MaiThailand
,
Pharuhus Chanprapaph Department of Obstetrics and Gynecology, Faculty of Medicine, Chiang Mai University, Chiang MaiThailand
,
Chanane Wanpirak Department of Obstetrics and Gynecology, Faculty of Medicine, Chiang Mai University, Chiang MaiThailand
,
Panaee Siriwatanapa Department of Obstetrics and Gynecology, Faculty of Medicine, Chiang Mai University, Chiang MaiThailand
,
Supatra Sirichotiyakul Department of Obstetrics and Gynecology, Faculty of Medicine, Chiang Mai University, Chiang MaiThailand
&
Gebhard Flatz Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang MaiThailand
 show all
Pages 19-27 | Received 25 May 2000, Accepted 03 Sep 2000, Published online: 07 Jul 2009

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Khushnooma Y. Italia, Pratibha M. Sawant, Anita H. Nadkarni, Kanjaksha Ghosh & Roshan B. Colah. (2012) Is the Poly A (T>C) Mutation a Causative Factor For Misdiagnosis in Second Trimester Prenatal Diagnosis of β-Thalassemia by Fetal Blood Analysis on High Performance Liquid Chromatography?. Hemoglobin 36:2, pages 114-123.
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Sakorn Pornprasert, Chutharat Kasemrad & Kanyakan Sukunthamala. (2010) Diagnosis of Thalassemia on Dried Blood Spot Samples by High Performance Liquid Chromatography. Hemoglobin 34:5, pages 486-494.
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Unthika Chamras, Kanyakan Sukunthamala & Sakorn Pornprasert. (2009) SYTO9 and SYBR Green1 with High Resolution Melting Analysis for Molecular Confirmatory Testing of the Common Southeast Asian β0-thalassemia Mutations. Hemoglobin 33:6, pages 539-545.
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Seema Rao, Renu Saxena, Deepika Deka & Madhulika Kabra. (2009) Use of HbA estimation by CE-HPLC for prenatal diagnosis of β-thalassemia; experience from a tertiary care centre in north India: a brief report. Hematology 14:2, pages 122-124.
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Supatra Sirichotiyakul, Rattika Saetung & Torpong Sanguansermsri. (2009) Prenatal Diagnosis of β-Thalassemia/Hb E by Hemoglobin Typing Compared to DNA Analysis. Hemoglobin 33:1, pages 17-23.
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S. Elgawhary, M. Y. Elbaradie Sahar, Wael M. Rashad, Maha Mosaad, M. A. H. Abdalla, G. Ezzat, Yassar A. Wali & A. Elbeshlawy. (2008) PRENATAL DIAGNOSIS OF β-THALASSEMIA IN EGYPT: Implementing Accurate High-Tech Methods Did not Reflect Much on the Outcome. Pediatric Hematology and Oncology 25:6, pages 541-548.
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Dongzhi Li, Can Liao, Jian Li & Xuewei Tang. (2006) The Codon 37 (TGG→TAG) β0-Thalassemia Mutation Found in a Chinese Family. Hemoglobin 30:2, pages 171-173.
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Articles from other publishers (10)

Dong-Zhi Li & Yan-Dong Yang. (2017) Invasive prenatal diagnosis of fetal thalassemia. Best Practice & Research Clinical Obstetrics & Gynaecology 39, pages 41-52.
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Sakorn Pornprasert, Monthathip Tookjai, Manoo Punyamung, Panida Pongpunyayuen & Kanokwan Jaiping. (2016) Development of hemoglobin typing control materials for laboratory investigation of thalassemia and hemoglobinopathies. Clinical Chemistry and Laboratory Medicine (CCLM) 54:1.
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Kasemsri Srisupundit, Chanane Wanapirak, Supatra Sirichotiyakul, Fuanglada Tongprasert, Suchaya Leuwan, Kuntharee Traisrisilp & Theera Tongsong. (2013) Hemoglobin levels and red blood cell indices in mid‐gestational fetuses with beta‐thalassemia/HbE, beta‐thalassemia trait or Hb E trait and normal fetuses. Prenatal Diagnosis 33:13, pages 1238-1241.
Crossref
Khushnooma Italia, Pratibha Sawant, Reema Surve, Marukh Wadia, Anita Nadkarni, Kanjaksha Ghosh & Roshan Colah. (2012) Variable haematological and clinical presentation of β‐thalassaemia carriers and homozygotes with the P oly A ( T → C ) mutation in the Indian population . European Journal of Haematology 89:2, pages 160-164.
Crossref
Sakorn Pornprasert & Kanyakan Sukunthamala. (2010) SYTO9 and SYBR GREEN1 with a high-resolution melting analysis for prenatal diagnosis of β0-thalassemia/hemoglobin-E. European Journal of Haematology 85:5, pages 424-429.
Crossref
Hataichanok Srivorakun, Goonnapa Fucharoen, Nattaya Sae-Ung, Kanokwan Sanchaisuriya, Thawalwong Ratanasiri & Supan Fucharoen. (2009) Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases. European Journal of Haematology 83:1, pages 57-65.
Crossref
Can Liao, Dong-Zhi Li & Jian Li. (2008) First detection of the codons 41–43 (−CTTTG,+A) β-thalassemia mutation in a Chinese patient. Annals of Hematology 87:9, pages 775-776.
Crossref
Dongzhi Li, Can Liao, Jian Li, Xingmei Xie, Yining Huang, Huizhu Zhong & Jiaxue Wei. (2006) Prenatal diagnosis of β-thalassemia in Southern China. European Journal of Obstetrics & Gynecology and Reproductive Biology 128:1-2, pages 81-85.
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Chunming DingRossa W. K. ChiuTze K. LauTse N. LeungLi C. ChanAmy Y. Y. ChanPimlak CharoenkwanIvy S. L. NgHai-yang LawEdmond S. K. MaXiangmin XuChanane WanapirakTorpong SanguansermsriCan LiaoMary Anne Tan Jin AiDavid H. K. ChuiCharles R. CantorY. M. Dennis Lo. (2004) MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis. Proceedings of the National Academy of Sciences 101:29, pages 10762-10767.
Crossref
Mahrukh R. Wadia, Supriya P. Phanasgaokar, Anita H. Nadkarni, Reema R. Surve, Ajit C. Gorakshakar, Roshan B. Colah & Dipika Mohanty. (2002) Usefulness of automated chromatography for rapid fetal blood analysis for second trimester prenatal diagnosis of β‐thalassemia. Prenatal Diagnosis 22:2, pages 153-157.
Crossref

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