- ►nih.gov [PDF] RF Trecartin, SA Liebhaber, JC Chang, … - Journal of clinical …, 1981 - pubmedcentral.nih.gov A BSTRA C T We report the characterization of a molecular lesion of (8 thalassemia in Sardinia. Beta
thalassemia in this area is predominantly the (80 type with low levels of,8-globin mRNA. Translation
assay of this messenger RNA in a ... Cited by 118 - Related articles - All 5 versions
N Ghanem, E Girodon, M Vidaud, J Martin, P Fanen, … - Hum Mutat, 1992 - interscience.wiley.com We describe a scanning procedure for the detection of -globin gene mutations and the prenatal
diagnosis of -thalassemias. The method is based on the combined use of PCR and denaturing gradient
gel electrophoresis (DGGE) of six ... Cited by 67 - Related articles - All 2 versions
- ►pnas.org [PDF] RE Kaufman, PJ Kretschmer, JW Adams, … - Proceedings of the …, 1980 - National Acad Sciences Page 1. Proc. Nat!. Acad. Sci. USA Vol. 77, No. 7, pp. 4229-423, July 1980 Genetics Cloning and
characterization of DNA sequences surrounding the human oy-, b-, and fl-globin genes (repetitive
DNA sequences/thalassemia/electron microscopy/Southern blot analysis) ... Cited by 43 - Related articles - All 7 versions
- ►hematologylibrary.org [PDF] BJ Padanilam, AE Felice, TH Huisman - Blood, 1984 - bloodjournal.hematologylibrary.org . Hematology; all rights reserved Copyright 2007 by The American Society of DC 20036. by the
American Society of Hematology, 1900 M St, NW, Suite 200, Washington Blood (print ISSN 0006-4971,
online ISSN 1528-0020), is ... Cited by 31 - Related articles - All 4 versions
MH Steinberg, JG Adams - The American journal of pathology, 1983 - pubmedcentral.nih.gov THE GENES that specify the structure and direct the synthesis of globin have been assigned to
specific chromosomal regions,"2 mapped by restriction en- donuclease analysis,3-6 and completely
sequenced.'-" The a and a-like ... Cited by 17 - Related articles - All 4 versions
CS Johnson, C Tegos, E Beutler - Archives of Internal Medicine, 1982 - archinte.highwire.org \s=b\\g=a\Thalassemiais common in southeast Asia and theMedi- terranean, where the predominant
lesion seems to be a deletion of one or more of the four gene loci responsible for \g=a\globin chain
production. In theUnited States, ... Cited by 16 - Related articles - All 3 versions
RS Olney - American journal of preventive medicine, 1999 - Elsevier Results: Most clinical interventions for people with sickle cell disease discussed in the medical
literature can be classified as tertiary prevention: for example, therapy to ameliorate anemia,
reduce the frequency of pain ... Cited by 14 - Related articles - BL Direct - All 7 versions
MH Steinberg, MB Coleman, JG Adams, O … - British journal of …, 1983 - ncbi.nlm.nih.gov In HbSC disease, as in sickle cell anaemia, there is a spectrum of clinical severity. A reduced mean
corpuscular volume and haemoglobin concentration, traits typical of thalassaemia, might retard
sickling. We therefore ascertained ... Cited by 14 - Related articles - All 2 versions
WC Mahoney, PE Nute - Biochemistry, 1980 - ncbi.nlm.nih.gov The complete amino acid sequence of the gamma chain from the major one of two fetal hemoglobins from
the rhesus monkey, Macaca mulatta, was determined by automated, stepwise degradation of selected
fragments produced by cleavage at ... Cited by 17 - Related articles - All 2 versions
MH Steinberg, JG Adams - Am J Hematol, 1982 - interscience.wiley.com It is also possible that your web browser is not configured or not able to display style sheets. In
this case, although the visual presentation will be degraded, the site should continue to be
functional. We recommend using the ... Cited by 10 - Related articles - All 2 versions
