Schirwani, Schaida <br/><br/>
Clinical and molecular characterization of the first familial report of 1p32 microdeletion.  [electronic resource] 

 -  Clinical dysmorphology  Apr 2018 
 - 36-41 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1473-5717 
<br/><br/><label>Standard No.: </label>10.1097/MCD.0000000000000209  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adult<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 1--genetics<br/>Comparative Genomic Hybridization<br/>DNA-Binding Proteins--genetics<br/>Developmental Disabilities--genetics<br/>Female<br/>Humans<br/>LDL-Receptor Related Proteins--genetics<br/>Male<br/>Microcephaly--genetics<br/>Pedigree<br/>Phenotype<br/>Transcription Factors--genetics