Ko, T M <br/><br/>
Prenatal diagnosis of Hb H disease due to compound heterozygosity for South-east Asian deletion and Hb constant spring by polymerase chain reaction.  [electronic resource] 

 -  Prenatal diagnosis  Feb 1993 
 - 143-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0197-3851 
<br/><br/><label>Standard No.: </label>10.1002/pd.1970130210  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abortion, Therapeutic<br/>Adult<br/>Base Sequence<br/>Blotting, Southern<br/>Chorionic Villi Sampling<br/>Chromosome Deletion<br/>DNA--analysis<br/>Female<br/>Fetal Diseases--diagnosis<br/>Heterozygote<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Pregnancy<br/>Pregnancy Trimester, First<br/>alpha-Thalassemia--diagnosis