Vissers, L E L M <br/><br/>
Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies.  [electronic resource] 

 -  Human genetics  Jul 2007 
 - 697-709 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s00439-007-0359-6  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Child<br/>Chromosome Aberrations<br/>Chromosome Breakage<br/>Chromosomes, Human, Pair 17--genetics<br/>Cytogenetics<br/>DNA--genetics<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Nucleic Acid Hybridization<br/>Oligonucleotide Array Sequence Analysis<br/>Pregnancy<br/>Repetitive Sequences, Nucleic Acid