Ferguson-Smith, M A <br/><br/>
Heterozygosity at the alpha-haptoglobin locus associated with a deletion, 16q22 leads to 16qter.  [electronic resource] 

 -  Cytogenetics and cell genetics  1978 
 - 513 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0301-0171 
<br/><br/><label>Standard No.: </label>10.1159/000131011  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Chromosome Deletion<br/>Chromosome Mapping<br/>Chromosomes, Human, 16-18<br/>Female<br/>Haptoglobins--genetics<br/>Heterozygote<br/>Humans