Rothnagel, J A <br/><br/>
Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis.  [electronic resource] 

 -  Prenatal diagnosis  Aug 1998 
 - 826-30 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0197-3851 
<br/><br/><label>Standard No.: </label>10.1002/(sici)1097-0223(199808)18:8<826::aid-pd360>3.0.co;2-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amniotic Fluid--cytology<br/>DNA Mutational Analysis<br/>DNA Restriction Enzymes<br/>Female<br/>Humans<br/>Hyperkeratosis, Epidermolytic--diagnosis<br/>Keratins--genetics<br/>Mosaicism<br/>Mutation<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Pregnancy<br/>Prenatal Diagnosis<br/>Sequence Analysis, DNA