Miniou, P <br/><br/>
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.  [electronic resource] 

 -  Human molecular genetics  Dec 1994 
 - 2093-102 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/3.12.2093  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>5-Methylcytosine<br/>Abnormalities, Multiple--genetics<br/>Base Sequence<br/>Case-Control Studies<br/>Centromere<br/>Child<br/>Chromosome Aberrations--genetics<br/>Chromosome Disorders<br/>Chromosomes, Human, Pair 1<br/>Chromosomes, Human, Pair 16<br/>Cytosine--analogs & derivatives<br/>DNA, Satellite<br/>Face--abnormalities<br/>Female<br/>Heterochromatin--metabolism<br/>Humans<br/>Immunologic Deficiency Syndromes--genetics<br/>Infant<br/>Male<br/>Methylation<br/>Molecular Sequence Data<br/>Syndrome<br/>X Chromosome