Chery, M <br/><br/>
Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint.  [electronic resource] 

 -  Human genetics  May 1994 
 - 587-91 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/BF00202829  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Blotting, Southern<br/>Cell Transformation, Viral<br/>Chromosome Aberrations<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 9<br/>Female<br/>Humans<br/>Hypocalcemia--complications<br/>In Situ Hybridization<br/>Magnesium Deficiency--complications<br/>Translocation, Genetic<br/>X Chromosome