Kiper, Pelin Özlem Şimşek <br/><br/>
Catel-Manzke syndrome: a clinical report suggesting autosomal recessive inheritance.  [electronic resource] 

 -  American journal of medical genetics. Part A  Sep 2011 
 - 2288-92 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.34163  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adult<br/>Chromosome Disorders--genetics<br/>Cleft Palate--genetics<br/>Consanguinity<br/>Female<br/>Genes, Recessive<br/>Hand Deformities, Congenital--genetics<br/>Humans<br/>Infant<br/>Male<br/>Pierre Robin Syndrome--genetics