The Codon 37 (TGG→TAG) β⁰-Thalassemia Mutation Found in a Chinese Family

Dongzhi Li Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of ChinaCorrespondence[email protected]

Can Liao Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China

Jian Li Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China

Xuewei Tang Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China

REFERENCES

Weatherall DJ, Clegg JB. The Thalassaemia Syndromes. 4th. Blackwell Scientific Publications, Oxford 2001
Google Scholar
Ko TM, Xu X. Molecular study and prenatal diagnosis of α- and β-thalassemias in Chinese. J Formos Med Assoc 1998; 97(1)5–15, [INFOTRIEVE], [CSA]
PubMed Web of Science ®Google Scholar
Kornblit B, Taaning P, Birgens H. β-Thalassemia due to a novel nonsense mutation at codon 37 (TGG→TAG) found in an Afghanistani family. Hemoglobin 2005; 29(3)209–213, [INFOTRIEVE], [CROSSREF], [CSA]
PubMed Web of Science ®Google Scholar
Fucharoen S, Winichagoon P, Wisedpanichkij R, Sae-Ngow B, Sriphanich R, Oncoung W, Muangsapaya W, Chowthaworn J, Kanokpongsakdi S, Bunyaratvej A, Piankijagum A, Dewaele C. Prenatal and postnatal diagnoses of thalassemias and hemoglobinopathies by HPLC. Clin Chem 1998; 44(4)740–748, [INFOTRIEVE], [CSA]
PubMed Web of Science ®Google Scholar
Tongsong T, Wanapirak C, Sirivatanapa P, Sanguansermsri T, Sirichotiyakul S, Piyamongkol W, Chanprapaph P. Prenatal control of severe thalassemia: Chiang Mai strategy. Prenat Diagn 2000; 20(3)229–234, [INFOTRIEVE], [CROSSREF], [CSA]
PubMed Web of Science ®Google Scholar
Sanguansermsri T, Thanarattanakorn P, Steger HF, Tongsong T, Chanprapaph P, Wanpirak C, Siriwatanapa P, Sirichotiyakul S, Flatz G. Prenatal diagnosis of β-thalassemia major by high performance liquid chromatography analysis of hemoglobins in fetal blood samples. Hemoglobin 2001; 25(1)19–27, [INFOTRIEVE], [CROSSREF], [CSA]
PubMed Web of Science ®Google Scholar
Huisman THJ, Carver MFH. The β- and δ-thalassemia repository (ninth edition; part I). Hemoglobin 1998; 22(2)169–195, [INFOTRIEVE], [CSA]
PubMed Web of Science ®Google Scholar

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

The Codon 37 (TGG→TAG) β⁰-Thalassemia Mutation Found in a Chinese Family

REFERENCES

Information for

Open access

Opportunities

Help and information

Your download is now in progress and you may close this window

Login or register to access this feature

The Codon 37 (TGG→TAG) β0-Thalassemia Mutation Found in a Chinese Family

REFERENCES

Reprints and Corporate Permissions

Academic Permissions

Related research

To cite this article:

Download citation

Information for

Open access

Opportunities

Help and information

Keep up to date

The Codon 37 (TGG→TAG) β⁰-Thalassemia Mutation Found in a Chinese Family