Khosla, S <br/><br/>
Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas.  [electronic resource] 

 -  The Journal of clinical investigation  May 1991 
 - 1691-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0021-9738 
<br/><br/><label>Standard No.: </label>10.1172/JCI115186  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adrenal Gland Neoplasms--genetics<br/>Adult<br/>Aged<br/>Alleles<br/>Carcinoma--genetics<br/>Child<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 10<br/>Chromosomes, Human, Pair 17<br/>Female<br/>Heterozygote<br/>Humans<br/>Male<br/>Middle Aged<br/>Pheochromocytoma--genetics<br/>Thyroid Neoplasms--genetics