home genetic news bioinformatics biotechnology literature journals ethics positions events sitemap


UBBFriend: Email This Page to Someone!
  HUM-MOLGEN
  DIAGnostics - Clinical Research (professional requests)
  X-linked reticulate pigmentary disorder

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

next newest topic | next oldest topic
Author Topic:   X-linked reticulate pigmentary disorder
azinn
Member
posted 01-29-2003 05:49 PM     Click Here to See the Profile for azinn   Click Here to Email azinn     Edit/Delete Message Reply w/Quote
Families with X-linked reticulate pigmentary disorder with systemic manifestations, also known as familial cutaneous amyloidosis with systemic manifestations in males or X-linked cutaneous amyloidosis, are needed for an IRB-approved study aimed at identifying the defective gene. If you have any patients with this disorder, please contact Dr. Andrew Zinn at (214) 648-1615 (Andrew.Zinn@UTSouthwestern.edu). Thank you.

------------------
Andrew R. Zinn, M.D., Ph.D.
Assistant Professor
UT Southwestern Med School
5323 Harry Hines Blvd.
Dallas, TX 75390-8591
USA
Tel (214) 648-1600
Fax (214) 648-1666
Andrew.Zinn@UTSouthwestern.edu

IP: 129.112.109.251

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 1995-2015

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.