Sophocleous, T <br/><br/>
The molecular basis for the haemoglobin Bart's hydrops fetalis syndrome in Cyprus.  [electronic resource] 

 -  British journal of haematology  Jan 1981 
 - 153-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0007-1048 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2141.1981.tb02770.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Aberrations<br/>Chromosome Disorders<br/>Chromosomes, Human, 16-18<br/>Cyprus<br/>Edema--genetics<br/>Female<br/>Fetal Diseases--genetics<br/>Fetal Hemoglobin--genetics<br/>Hemoglobins, Abnormal--genetics<br/>Homozygote<br/>Humans<br/>Male<br/>Pregnancy<br/>Syndrome