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Items: 1 to 20 of 131

1.

Molecular diagnosis of haemoglobin disorders.

Clark BE, Thein SL.

Clin Lab Haematol. 2004 Jun;26(3):159-76. Review.

PMID:
15163314
2.

Screening and genetic diagnosis of haemoglobin disorders.

Old JM.

Blood Rev. 2003 Mar;17(1):43-53. Review.

PMID:
12490210
3.

Screening and genetic diagnosis of haemoglobinopathies.

Old JM.

Scand J Clin Lab Invest. 2007;67(1):71-86. Review.

PMID:
17365985
4.

Application of diagnostic methods and molecular diagnosis of hemoglobin disorders in Khuzestan province of Iran.

Fakher R, Bijan K, Taghi AM.

Indian J Hum Genet. 2007 Jan;13(1):5-15. doi: 10.4103/0971-6866.32028.

5.

Laboratory investigation of hemoglobinopathies and thalassemias: review and update.

Clarke GM, Higgins TN.

Clin Chem. 2000 Aug;46(8 Pt 2):1284-90. Review.

6.

Genetic predisposition to β-thalassemia and sickle cell anemia in Turkey: a molecular diagnostic approach.

Basak AN, Tuzmen S.

Methods Mol Biol. 2011;700:291-307. doi: 10.1007/978-1-61737-954-3_19.

PMID:
21204041
7.

Complex interactions of deltabeta hybrid haemoglobin (Hb Lepore-Hollandia) Hb E (beta(26G-->A)) and alpha+ thalassaemia in a Thai family.

Viprakasit V, Pung-Amritt P, Suwanthon L, Clark K, Tanphaichtr VS.

Eur J Haematol. 2002 Feb;68(2):107-11.

PMID:
12038449
8.

Haemoglobinopathies.

Old J.

Prenat Diagn. 1996 Dec;16(13):1181-6. Review.

PMID:
9061749
9.

Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China.

Xiong F, Sun M, Zhang X, Cai R, Zhou Y, Lou J, Zeng L, Sun Q, Xiao Q, Shang X, Wei X, Zhang T, Chen P, Xu X.

Clin Genet. 2010 Aug;78(2):139-48. doi: 10.1111/j.1399-0004.2010.01430.x. Epub 2010 Apr 19.

PMID:
20412082
10.

Prenatal diagnosis and screening of the haemoglobinopathies.

Cao A, Galanello R, Rosatelli MC.

Baillieres Clin Haematol. 1998 Mar;11(1):215-38. Review.

PMID:
10872479
11.

Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies.

Patrinos GP, Kollia P, Papadakis MN.

Hum Mutat. 2005 Nov;26(5):399-412. Review.

PMID:
16138310
12.

Clinical and molecular aspects of haemoglobinopathies in Tunisia.

Haj Khelil A, Laradi S, Miled A, Omar Tadmouri G, Ben Chibani J, Perrin P.

Clin Chim Acta. 2004 Feb;340(1-2):127-37.

PMID:
14734204
13.

Haemoglobin Hope in a northern Thai family: first identification of homozygous haemoglobin Hope associated with haemoglobin H disease.

Sura T, Busabaratana M, Youngcharoen S, Wisedpanichkij R, Viprakasit V, Trachoo O.

Eur J Haematol. 2007 Sep;79(3):251-4. Epub 2007 Jul 26.

PMID:
17655700
14.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
15.

Diagnostic approach to hemoglobinopathies.

Kutlar F.

Hemoglobin. 2007;31(2):243-50.

PMID:
17486507
16.

Carrier screening and prenatal diagnosis of hemoglobinopathies. A study of indigenous and immigrant couples in northern Greece, over the last 5 years.

Theodoridou S, Alemayehou M, Prappas N, Karakasidou O, Aletra V, Plata E, Tsaftaridis P, Karababa P, Boussiou M, Sinopoulou K, Hatzi A, Voskaridou E, Loutradi A, Manitsa A.

Hemoglobin. 2008;32(5):434-9. doi: 10.1080/03630260802341745.

PMID:
18932067
17.

Newborn screening for non-sickling hemoglobinopathies.

Hoppe CC.

Hematology Am Soc Hematol Educ Program. 2009:19-25. doi: 10.1182/asheducation-2009.1.19. Review.

PMID:
20008178
18.

Transcervical cells and the prenatal diagnosis of haemoglobin (Hb) mutations.

Cirigliano V, Sherlock J, Petrou M, Ward RH, Rodeck C, Adinolfi M.

Clin Genet. 1999 Nov;56(5):357-61.

PMID:
10668925
19.

Thalassemia and related hemoglobinopathies.

Sarnaik SA.

Indian J Pediatr. 2005 Apr;72(4):319-24. Review.

PMID:
15876761
20.

Antenatal diagnosis of haemoglobinopathies by Biorex chromatography of haemoglobin.

Blouquit Y, Beuzard Y, Varnavides L, Chabret C, Dumez Y, John PN, Rodeck C, White JM.

Br J Haematol. 1982 Jan;50(1):7-15.

PMID:
6173058

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