HUM-MOLGEN archive: UNSUBSCRIBE, please stop sending messageS!!!!!!!!

**************************************************** HUM-MOLGEN DIAGnostics/Clinical Research **************************************************** This DIAG message contains 7 patient requests and 1 submessage: 1) CADASIL (pt request) 2) Genetic research on native Americans (pt request) 3) Partial deletion of chromosome 9 (pt request) 4) Von Willebrandt disease (pt request) 5) Malignant melanoma (pt request) 6) Genetic aspects of behaviour (pt request) 7) Fetal cells in maternal blood (pt request) 8) Fructose-1,6-bisphosphatase deficiency ***************************************************** Carlo Gambacorti, MD, Editor, Min Ae Lee, MD, Assistant Editor Human Molecular Genetics Network Diagnostics/Clinical Research Section ***************************************************** ***************************************************** 1) CADASIL Pt request - please reply directly to Hum-Molgen ! Apparent pt location: Mexico Well, I am writing from Mexico City, exactlym from the Tecnological Institute from which I am a student. About 2 weeks ago my mother told us that my father had the CADASIL DISEASE and she also told us that she almost know nothing about it. This was a diagnosis given by a Neurological Clinic on Rochester, New York, in the US. Many doctors here in Mexico have almost the same information we have and there are some that sweared it was the first time they heard about it. As you can see, we are ignorant about this disease and we would like(my family and I) you to send us some information about it, whatever you have. ***************************************************** 2) Genetic research on native americans Pt request - please reply directly to Hum-Molgen ! Apparent pt location: USA I am interested in genetic research on native americans. Also please provide information about sponsoring your research. thank you, ***************************************************** 3) Partial deletion of chromosome 9 Pt request - please reply directly to Hum-Molgen ! Apparent pt location: Luxemburg Dear sir, Do you know if there are any physical and mental consequences for a foetus when one of the chromosom of the paire 9 doesn't have the centronic heterochromatin? thanks a lot for your help Best regards ***************************************************** 4) Von Willebrandt disease Pt request - please reply directly to Hum-Molgen ! Apparent pt location: USA i am a 21 year old female who has endured the misery of this disorder since 13 years of age. i really would appreciate any referrals someone can give in the Dallas area (or anywhere for that matter). THANKS for any help!! ***************************************************** 5) Malignant melanoma Pt request - please reply directly to Hum-Molgen ! Apparent pt location: USA What is the current medical treatment or trials occurring within the U.S. for malignent melanoma found in the lungs? To whom should one contact in order to get the latest information on clinical trials for this particular type of cancer? ***************************************************** 6) Genetic aspects of behaviour Pt request - please reply directly to Hum-Molgen ! Apparent pt location: USA Simply I am writing a paper for my Psychology class and am interested in researching the topic of genetic influence on personality traits. I would greatly appreciate any time a person could spend on sending me any information. The material I have been able to obtain is substancial, however I would like to broaden my knowledge and their for perspective on the subjest. Thank you for your time. ***************************************************** 7) Fetal cells in maternal blood Pt request - please reply directly to Hum-Molgen ! Apparent pt location: Brasil Hello,I'm looking for person who worked with fetal cells in maternal blood. Can you help me???Thank you in advance, ***************************************************** 8) Fructose-1,6-bisphosphatase deficiency Dear colleagues, Herewith I would like to inform you that we set up a DNA-based method to detect the molecular origin of fructose-1,6-bisphosphatase deficiency in the patients we care for. It would be very interesting for us to apply the method also to material from other patients. All what we need is about 3 ml of EDTA-blood, sent by ordinary mail (within Europe) or Air mail (outside Europe) together with some basic data about the clinical status. If you yourself take care for patients with fructose-1,6-bisphosphatase deficiency, I would be very grateful to you if you contacted me. Though material from clinically and biochemically well diagnosed patients is preferred, also material from doubtful cases is welcome. You will be informed about the results of the analysis without delay. If you know a colleague who might be able and willing to let us have material, please be so kind to inform him about our work. If possible, please let me know his address so that I could also contact him directly. Please don't hesitate to contact me for any further information. Klaus Eschrich Prof. Dr. Klaus Eschrich Institut fuer Biochemie Universitaet Leipzig Liebigstr. 16 D-04103 Leipzig Tel.: 49-0341-9722105 Fax: 49-0341-9722109 oder 49-0341-9722119 E-Mail: eschrich@rz.uni-leipzig.de ***************************************************** HUM-MOLGEN - Internet Communication Forum in Human Genetics E-mail: HUM-MOLGEN@nic.surfnet.nl WWW: http://www.informatik.uni-rostock.de/HUM-MOLGEN/ Phone: 020-566 4598 (The Netherlands), (206) 386-2101 (USA) Fax: 020-691 6521 (The Netherlands), (206) 386-2555 (USA) ---------------------------------------------------------------------------- ----------------- "copyright HUM-MOLGEN"