Hjelle, B <br/><br/>
Hemoglobin H disease and multiple congenital anomalies in a child of northern European origin.  [electronic resource] 

 -  American journal of hematology  Dec 1982 
 - 319-22 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0361-8609 
<br/><br/><label>Standard No.: </label>10.1002/ajh.2830130407  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--blood<br/>Child<br/>DNA--genetics<br/>Genotype<br/>Hemoglobin H--analysis<br/>Humans<br/>Male<br/>Nucleic Acid Hybridization<br/>Pedigree<br/>Thalassemia--blood