Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 The molecular basis for the haemoglobin Bart's hydrops fetalis syndrome in Cyprus.

× No keyword cloud information.

6 in total

1. Prenatal diagnosis of alpha-thalassemia by polymerase chain reaction and dual restriction enzyme analysis.

Authors: R V Lebo; R K Saiki; K Swanson; M A Montano; H A Erlich; M S Golbus
Journal: Hum Genet Date: 1990-08 Impact factor: 4.132

2. Genetic and molecular diversity in nondeletion Hb H disease.

Authors: D R Higgs; L Pressley; B Aldridge; J B Clegg; D J Weatherall; A Cao; M G Hadjiminas; C Kattamis; A Metaxatou-Mavromati; E A Rachmilewitz; T Sophocleous
Journal: Proc Natl Acad Sci U S A Date: 1981-09 Impact factor: 11.205

Review 3. The thalassemias: molecular mechanisms of human genetic disease.

Authors: R A Spritz; B G Forget
Journal: Am J Hum Genet Date: 1983-05 Impact factor: 11.025

4. Human alpha-globin gene expression is silenced by terminal truncation of chromosome 16p beginning immediately 3' of the zeta-globin gene.

Authors: L Romao; F Cash; I Weiss; S Liebhaber; M Pirastu; R Galanello; A Loi; E Paglietti; P Ioannou; A Cao
Journal: Hum Genet Date: 1992-05 Impact factor: 4.132

5. Homozygosity for the Mediterranean a-thalassemic deletion (hemoglobin Barts hydrops fetalis).

Authors: Nasir A S Al-Allawi; Maida Y Shamdeen; Najeeb S Rasheed
Journal: Ann Saudi Med Date: 2010 Mar-Apr Impact factor: 1.526

6. An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotype.

Authors: P Moi; F E Cash; S A Liebhaber; A Cao; M Pirastu
Journal: J Clin Invest Date: 1987-11 Impact factor: 14.808

6 in total