Stoppoloni, G <br/><br/>
Seckel syndrome: report of three sibships with the type I primordial dwarfism. Possible linkage with HLA locus.  [electronic resource] 

 -  Annales de genetique  1992 
 - 213-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0003-3995 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Child<br/>Dwarfism--genetics<br/>Female<br/>Genetic Linkage<br/>HLA Antigens--genetics<br/>Haplotypes<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Pedigree<br/>Puberty, Precocious--genetics<br/>Syndrome