Spengler, Sabrina <br/><br/>
Molecular karyotyping as a relevant diagnostic tool in children with growth retardation with Silver-Russell features.  [electronic resource] 

 -  The Journal of pediatrics  Nov 2012 
 - 933-42 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1097-6833 
<br/><br/><label>Standard No.: </label>10.1016/j.jpeds.2012.04.045  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Child, Preschool<br/>Chromosome Aberrations<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 11--genetics<br/>Chromosomes, Human, Pair 7--genetics<br/>Female<br/>Genetic Markers--genetics<br/>Growth Disorders--diagnosis<br/>Humans<br/>Infant<br/>Karyotyping--methods<br/>Male<br/>Mutation<br/>Oligonucleotide Array Sequence Analysis<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>Silver-Russell Syndrome--diagnosis