Wirtz, M K <br/><br/>
Weill-Marchesani syndrome--possible linkage of the autosomal dominant form to 15q21.1.  [electronic resource] 

 -  American journal of medical genetics  Oct 1996 
 - 68-75 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/(SICI)1096-8628(19961002)65:1<68::AID-AJMG11>3.0.CO;2-P  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, Pair 15<br/>Dwarfism--genetics<br/>Eye Abnormalities--genetics<br/>Female<br/>Fibrillin-1<br/>Fibrillins<br/>Genes, Dominant<br/>Genetic Linkage<br/>Humans<br/>Immunologic Techniques<br/>Infant<br/>Male<br/>Microfilament Proteins--genetics<br/>Microsatellite Repeats<br/>Middle Aged<br/>Pedigree<br/>Syndrome