Bravo-Gil, Nereida <br/><br/>
Expanding the clinical and mutational spectrum of germline ABL1 mutations-associated syndrome: A case report.  [electronic resource] 

 -  Medicine  Mar 2019 
 - e14782 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1536-5964 
<br/><br/><label>Standard No.: </label>10.1097/MD.0000000000014782  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Diagnosis, Differential<br/>Germ-Line Mutation<br/>Humans<br/>Infant<br/>Male<br/>Phenotype<br/>Proto-Oncogene Proteins c-abl--genetics<br/>Syndrome