Armstrong, Linlea <br/><br/>
A boy with developmental delay, malformations, and evidence of a connective tissue disorder: possibly a new type of cutis laxa.  [electronic resource] 

 -  American journal of medical genetics. Part A  May 2003 
 - 57-62 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.10175  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Bone and Bones--diagnostic imaging<br/>Child<br/>Child, Preschool<br/>Connective Tissue Diseases--genetics<br/>Cutis Laxa--genetics<br/>Cytogenetic Analysis<br/>Dermis--pathology<br/>Developmental Disabilities--genetics<br/>Hand Deformities, Congenital--diagnostic imaging<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Microscopy, Electron<br/>Radiography