Leclercq, Sandrine <br/><br/>
Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model.  [electronic resource] 

 -  American journal of medical genetics. Part A  Mar 2009 
 - 437-45 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.32640  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Aberrations<br/>Chromosome Breakage<br/>Chromosome Disorders--genetics<br/>Chromosome Inversion<br/>Chromosomes, Artificial, Bacterial<br/>Chromosomes, Human, Pair 20--genetics<br/>Cytogenetic Analysis<br/>Developmental Disabilities--genetics<br/>Fluorescent Dyes--metabolism<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Indoles--metabolism<br/>Infant<br/>Intellectual Disability--genetics<br/>Karyotyping<br/>Male<br/>Models, Genetic<br/>Nucleic Acid Hybridization<br/>Recombination, Genetic<br/>Trisomy