Fryns, J P <br/><br/>
Osteopenia, abnormal dentition, hydrops fetalis and communicating hydrocephalus: unusual early clinical signs in Coffin-Lowry syndrome.  [electronic resource] 

 -  Clinical genetics  Aug 1996 
 - 112 p.  digital 
<br/><br/> Publication Type: Case Reports; Comment; Letter 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.1996.tb02362.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--classification<br/>Bone Diseases, Metabolic--genetics<br/>Child, Preschool<br/>Face--abnormalities<br/>Fingers--abnormalities<br/>Humans<br/>Hydrocephalus--genetics<br/>Hydrops Fetalis--genetics<br/>Male<br/>Syndrome<br/>Tooth Abnormalities--genetics