Konialis, Christopher <br/><br/>
Uncovering recurrent microdeletion syndromes and subtelomeric deletions/duplications through non-selective application of a MLPA-based extended prenatal panel in routine prenatal diagnosis.  [electronic resource] 

 -  Prenatal diagnosis  Jun 2011 
 - 571-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Evaluation Study; Journal Article 
<br/><br/><label>ISSN: </label>1097-0223 
<br/><br/><label>Standard No.: </label>10.1002/pd.2750  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Chorionic Villi Sampling--statistics & numerical data<br/>Chromosome Aberrations--statistics & numerical data<br/>Chromosome Deletion<br/>Comparative Genomic Hybridization<br/>Diagnostic Tests, Routine--methods<br/>Female<br/>Gene Duplication<br/>Humans<br/>Incidence<br/>Karyotyping<br/>Male<br/>Nucleic Acid Amplification Techniques--methods<br/>Pregnancy<br/>Prenatal Diagnosis--methods<br/>Recurrence<br/>Syndrome<br/>Telomere--genetics