home genetic news bioinformatics biotechnology literature journals ethics positions events sitemap


UBBFriend: Email This Page to Someone!
   HUM-MOLGEN
  DIAGnostics - Clinical Research (professional requests)
  Schnyder's Crystalline Corneal Dystrophy (SCCD)

Post New Topic  Post A Reply
profile | register | preferences | faq | search

next newest topic | next oldest topic
Author Topic:   Schnyder's Crystalline Corneal Dystrophy (SCCD)
Jennifer Cox
Member 		posted 07-31-2001 07:05 PM     Click Here to See the Profile for Jennifer Cox   Click Here to Email Jennifer Cox     Edit/Delete Message Reply w/Quote
Dear Colleagues,

We are looking for the genetic variations that cause Schnyder’s Crystalline Corneal Dystrophy (SCCD). We are looking for additional individuals with SCCD to obtain blood/DNA and general history information from them and their families.


Jayne S. Weiss, M.D.
Helena Kuivaniemi, M.D., Ph.D.
Center for Molecular Medicine and Genetics
Wayne State University School of Medicine
3106 Scott Hall
540 E. Canfield
Detroit, MI 48201
(313) 577- 8733
kuivan@sanger.med.wayne.edu

IP: 146.9.113.115

All times are ET (US)

next newest topic | next oldest topic

Administrative Options: Close Topic | Archive/Move | Delete Topic
Post New Topic  Post A Reply
Hop to:

Contact Us | HUM-MOLGEN

Copyright by HUM-MOLGEN 1995-2017

Powered by: Ultimate Bulletin Board, Version 5.44a
© Infopop Corporation (formerly Madrona Park, Inc.), 1998 - 2000.

By posting requests at HUM-MOLGEN you reach more than 9.500 mailing list subscribers and a 6 digit number of www users. Therefore post high quality messages only, including full name and institutional address.