Disteche, C M <br/><br/>
X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes.  [electronic resource] 

 -  Human genetics  1984 
 - 71-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/BF00275190  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Chromosome Banding<br/>Chromosomes, Human, 16-18<br/>Chromosomes, Human, 21-22 and Y<br/>Chromosomes, Human, 6-12 and X<br/>Dosage Compensation, Genetic<br/>Female<br/>Fibroblasts--ultrastructure<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Karyotyping<br/>Lymphocytes--ultrastructure<br/>Phenotype<br/>Sex Chromosome Aberrations--genetics<br/>Skin--cytology<br/>Translocation, Genetic<br/>X Chromosome