TO: MEMBERS OF THE CYSTIC FIBROSIS GENETIC ANALYSIS CONSORTIUM
Amos, Boston U, USA Kalaydjieva, Sofia, Bulgaria
Anvret, Stockholm, Sweden Kant, U Penn, USA
Baranov, Leningrad, USSR Kerem, Jerusalem, Israel
Barker, U Alabama Birm, USA Kitzis, CHU-Paris, France
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Beaudet, Baylor, USA Knight, London, England
Boué, Paris, France Komel, Ljubljiana, Yugoslavia
Cao, U Cagliari, Italy Krueger, Hahnemann, USA
Carbonara, Torino, Italy Lavinha, Lisboa Codex, Portugal
Cassiman, U Leuven, Belgium Lissens, Vrije U Brussels, Belgium
Claustres, Montpellier, France Loukopoulos, Athens, Greece
Cochaux, Brussels, Belgium Lucotte, College de France
Collins, U Michigan, USA Malcolm, ICH-London, England
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Elles, St Mary's-Manchester, England Ramsay, SAMIR, South Africa
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Harris, Guy's-London, England Super, Royal Manchester, England
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Highsmith, NC Mem Hosp, USA Tümmler, Hannova, West Germany
Hood, California Inst Tech, USA Verellen-Dumoulin,Bruxelles,Belgium
Horst, Münster, West Germany Willems, U Antwerp, Belgium
Jaume-Roig, Son Dureta, Spain Williamson,St Mary'sLondon,England
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FROM: LAP-CHEE TSUI TOTAL NUMBER OF PAGES: 8
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NEWSLETTER #32, March 10, 1991
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1. Romeo G, Ronchetto P, Telleria JJ, Devoto M, Fanen P, and Goossens M report two mutations:
- a C to T transition at position 3604 in exon 19 (R1158X), and
- an A to G transition at position 3849+4 (a possible splice mutation); see attached letter.
2. A list of CF mutation is attached. I have included the Newsletter issue number in the reference. Please check the information for possible typing errors (I thank those who pointed them out to me in the past). Please also let me know if there is any update of the reference list (ie. paper accepted, etc.).
3. I would like to remind all members that any secondary publication resulted from knowledge of unpublished consortium data should obtain permission from the original reporting group to publish the information before submission. Also, although the original report may be published by the time the secondary paper is submitted, an acknowledgement is still appropriate if the research is based on unpublished information. This guideline applies to mutations, any sequence information (polymorphisms) and patient description.
4. It just came to my attention that several of the previous newsletters were sent in a reduced size. It was due to a sticky switch in the FAX machine (certainly not our intention to save money). I apologize for any inconvenience there might be.
Best regards,
Lap-Chee Tsui