Wolff, D J <br/><br/>
Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.  [electronic resource] 

 -  American journal of human genetics  Jul 1994 
 - 87-95 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.; Review 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Centromere--ultrastructure<br/>Child<br/>Child, Preschool<br/>Chromosome Aberrations--genetics<br/>Chromosome Disorders<br/>Chromosome Mapping<br/>Dosage Compensation, Genetic<br/>Female<br/>Gene Deletion<br/>Genetic Markers<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Intellectual Disability--genetics<br/>Karyotyping<br/>Male<br/>Mosaicism<br/>Phenotype<br/>RNA, Long Noncoding<br/>RNA, Untranslated<br/>Ring Chromosomes<br/>Telomere<br/>Transcription Factors--biosynthesis<br/>X Chromosome--ultrastructure