CFTR molecular screening

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Author	Topic: CFTR molecular screening
mtm Member	posted 03-14-2002 03:53 PM Is there anyone interested on mutation detection on CFTR patients originating from the Middle East with variable phenotypic expression? Haleh Akhavan-Niaki Genetic laboratory Amirkola Children Hospital Babol , Amirkola IRAN IP: 62.217.110.116
RobertoColombo unregistered	posted 03-19-2002 08:26 AM quote: Originally posted by mtm: Is there anyone interested on mutation detection on CFTR patients originating from the Middle East with variable phenotypic expression? Haleh Akhavan-Niaki Genetic laboratory ----------------------------------------- Dear Dr. Haleh Akhavan-Niaki In my lab we would be interested in performing CFTR mutation analysis on DNA samples from your patients. However, in order to take a final decision, it would be useful to receive from you further information on the number of patients, the presence of more than one patient in the pedegree (if any), and the main features of the phenotypes observed. Looking forward to a possible interesting and fruitful collaboration, with best regards Roberto Colombo, PhD Associate Professor Head Human Biology and Genetics Research Unit Department of Psychology Catholic University of the Sacred Heart Largo A. Gemelli 1 I-20123 Milan Italy Tel: +39 02 7234 2284 Fax: +39 02 7234 2280 email: rcolombo@mi.unicatt.it Amirkola Children Hospital Babol , Amirkola IRAN IP: 193.205.55.112
Wildhardt Member	posted 03-26-2002 09:51 AM Dear Dr. Haleh Akhavan-Niaki, we would like to offer you our spectrum of diagnostic CF tests for your patients. To implement such a study we would need additional information e.g. on the expected number of probes and on the main clinical features of the involved patients. our lab has extensive experience in taking care of foreign probes and we offer a wide range of diagnostic service to Middle East countries. Looking forward to a fruitful collaboration, with best regards, Gabi Wildhardt, Ph.D. Human Genetics & Molecular Biology Bioscientia Konrad-Adenauer-Str. 17 55218 Ingelheim, Germany Phone: +49-6132-781429 Fax: +49-6132-781466 email: GabrieleW@bioscientia.de ------------------ Dr. Gabriele Wildhardt IP: 195.96.33.203
Wildhardt Member	posted 03-26-2002 10:26 AM quote: Originally posted by mtm: Is there anyone interested on mutation detection on CFTR patients originating from the Middle East with variable phenotypic expression? Haleh Akhavan-Niaki Genetic laboratory Dear Dr. Haleh Akhavan-Niaki, we would like to offer you our spectrum of diagnostic CF tests for your patients. To implement such a study we would need additional information e.g. on the expected number of probes and on the main clinical features of the involved patients. our lab has extensive experience in taking care of foreign probes and we offer a wide range of diagnostic service to Middle East countries. Looking forward to a fruitful collaboration, with best regards, Gabi Wildhardt, Ph.D. Human Genetics & Molecular Biology Bioscientia Konrad-Adenauer-Str. 17 55218 Ingelheim, Germany Phone: +49-6132-781429 Fax: +49-6132-781466 email: GabrieleW@bioscientia.de Amirkola Children Hospital Babol , Amirkola IRAN ------------------ Dr. Gabriele Wildhardt IP: 195.96.33.203
Gnovelli Member	posted 07-23-2002 08:44 AM quote: Originally posted by RobertoColombo: We would like to offer you our CFTR screening using DHPLC mutation detection. Please let me know further information. Giuseppe Novelli novelli@med.uniroma2.it ------------------ IP: 160.80.52.144
majid11 Member	posted 09-18-2002 09:10 AM quote: Originally posted by mtm: Is there anyone interested on mutation detection on CFTR patients originating from the Middle East with variable phenotypic expression? Haleh Akhavan-Niaki Genetic laboratory Amirkola Children Hospital Babol , Amirkola IRAN -------------------------------------- Dear Dr.Haleh Akhavan-Niaki I am a student of Tehran university of medical sciences, school of public health, MS of human genetics. My dessertation is about Cystic Fibrosis mutations in Iranian population. I would be glad to collabrate with you.please let me know further information. Thank you. Majid Mojarrad Tehran university of medical sciences,School of public health, department of human genetics. Email: majid11@sphtums.com Tel:8003539-41 [This message has been edited by majid11 (edited 09-18-2002).] [This message has been edited by majid11 (edited 09-18-2002).] IP: 213.29.19.4
mehrdad NORUZI unregistered	posted 04-24-2003 06:21 PM dear Dr. Haleh Akhavan-Niaki our lab is one of the reference lab in Cf diagnosis in France and contributed to new mutation detection and specialized in this area please let me know more about your population : the number, ethnic Group etc you can directly mail me to mehrdad.noruzinia@igh.cnrs.fr laboratoire de G�n�tique Moleculaire chef: Pr CLAUSTRES IURC Montpellier France IP: 194.167.35.170
Keiles Member	posted 05-03-2003 03:21 AM At Ambry Genetics, we are able to do a modified gene scanning technique followed by direct sequence confirmation. We are able to detect over 1000 mutations and have been offering the test clinically for the last year. We accept samples from all over the world. Our current cost is $495 US dollars and our turnaround time is 2-3 weeks. If you are interested in possibly sending patient samples feel free to contact me directly. Steve ------------------ Steven Keiles, MS Ambry Genetics Corp. Costa Mesa, Ca. 92627 949-642-7202 IP: 63.206.251.2

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