Fernández, Raquel M <br/><br/>
Interstitial 10p deletion derived from a maternal ins(16;10)(q22;p13p15.2): Report of the first familial case of 10p monosomy affecting to two familial members of different generations.  [electronic resource] 

 -  American journal of medical genetics. Part A  May 2016 
 - 1268-73 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.37559  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>Chromosome Deletion<br/>Chromosome Disorders--genetics<br/>Chromosomes, Human, Pair 10--genetics<br/>Comparative Genomic Hybridization<br/>Developmental Disabilities--genetics<br/>DiGeorge Syndrome--genetics<br/>Gene Deletion<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Hypoparathyroidism--genetics<br/>In Situ Hybridization, Fluorescence<br/>Karyotyping<br/>Male<br/>Nephrosis--genetics