Niikawa, N <br/><br/>
Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2.  [electronic resource] 

 -  Human genetics  Sep 1991 
 - 561-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/BF00209012  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Aberrations<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 21<br/>Crossing Over, Genetic<br/>Down Syndrome--complications<br/>Female<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Myeloproliferative Disorders--complications<br/>Polymorphism, Restriction Fragment Length<br/>Syndrome