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Martin Kennedy: LITE: Contents HMG Vol 4 - Annual Review Issue | ||||||||||||||||
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To: Multiple recipients of list HUM-MOLGEN <HUM-MOLGEN@NIC.SURFNET.NL> Subject: LITE: Contents HMG Vol 4 - Annual Review Issue From: Martin Kennedy <MKENNEDY@chmeds.ac.nz> Date: Mon, 18 Sep 1995 10:32:05 +1200 Date sent: 18-SEP-1995 10:29:57 ============================================================== Human Molecular Genetics - ISSN 1964-6906 Volume 4, Annual Review Issue ============================================================== [For more information about how to obtain a copy of the 1995 annual review issue of Human Molecular Genetics, please see the SPECIAL ANNOUNCEMENTS below] ============================================================== Executive Editors:- K E Davies, Oxford, UK Huntington F Willard, Cleveland, OH, USA ============================================================== CONTENTS ============================================================== Recent molecular advances in dysmorphology R M Winter P. 1699 Syndromal mental retardation due to mutations in a regulator of gene expression R J Gibbons, D J Picketts and D R Higgs P. 1705 Dystrophin-associated proteins in muscular dystrophy E Ozawa, M Yoshida, A Suzuki, Y Mizuno, Y Hagiwara and S Noguchi P. 1711 PAX genes: what's new in developmental biology and cancer? E T Stuart and P Gruss P. 1717 Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy H Watkins, J G Seidman and C E Seidman P. 1721 Norrie disease and MAO genes-nearest neighbors Z-Y Chen, R M Denney and X O Breakefield P. 1729 Molecular genetics of retinitis pigmentosa T P Dryja and T Li P. 1739 Autosomal dominant polycystic kidney disease: molecular analysis P C Harris, C J Ward, B Peral and J Hughes P. 1745 DNA methylation in early development A Razin and R Shemer P. 1751 Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis D H Ledbetter and E Engel P. 1757 Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals B D Hendrich and H F Willard P. 1765 Compartmentalization of specific pre-mRNA metabolism: an emerging view P T Moen, Jr, K P Smith and J B Lawrence P. 1779 Disorders of peroxisome biogenesis N Braverman, G Dodt, S J Gould and D Valle P. 1791 Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders H C Dietz and R E Pyeritz P. 1799 Inherited breast and ovarian cancer C I Szabo and M-C King P. 1811 ============================================================== Human Molecular Genetics is a monthly journal of original peer-reviewed research, published by Oxford University Press. In addition to the regular monthly issues, a special review issue, reviewing important developments in the field, is published each year. The papers listed above will appear in the 1995 review issue, which is shortly to be printed. Copies are scheduled for despatch to subscribers on the 30 September 1995. SPECIAL ANNOUNCEMENTS 1. This annual review issue (contents listed above) will be sent automatically to you if you are a current subscriber to Human Molecular Genetics - it is part of your subscription. 2. Copies of this annual review issue are also available separately at US$20 (12.50 Pounds Sterling in Europe). If you would like an order form for this, please contact us - see contact details below. 3. If you are not currently a subscriber to Human Molecular Genetics, but intend to subscribe in 1996, then you can receive the 1995 annual review issue at no charge. All you need to do is: a) Ask us for a 1996 Human Molecular Genetics subscription order form b) Mention that you heard about this offer on the HUM- MOLGEN mailing list c) Send us your subscription order for a 1996 subscription, using the subscription order form which we send you In our turn we will: a) Send you a copy of the 1995 review issue at no charge, as soon as it is available in October 1995. b) Send you every month in 1996 your own personal copy of each regular issue of Human Molecular genetics, plus the 1996 review issue. You can contact us via any of the methods listed below: Mail: Journals Customer Services Oxford University Press Walton Street Oxford OX2 6DP United Kingdom Tel: +44 1865 267907 (or call free on 1-800-852-7323 in the USA and Canada) Fax: +44 1865 267485 E-Mail: jnlorders@oup.co.uk In addition, if you are attending the ASHG meeting in Minneapolis next month, we do hope you will visit the Oxford University Press exhibition stand. We hope to have copies of the Human Molecular Genetics 1995 review issue on display as well as copies of the regular October issue. ========================================= Copyright in the table of contents listed above is held by Oxford University Press, but you are welcome to circulate them further, provided that Oxford University Press is credited as publisher and copyright holder. 8< ======================= cut here ======================= >8 Cheers, Martin Kennedy (Standing in for Arthur Bergen, LITE Editor, HUMOLGEN) NNNN NN Martin A Kennedy (E-mail = mkennedy@chmeds.ac.nz) ZZZZZZZ NN NN NN Cytogenetic and Molecular Oncology Unit ZZZ NN NN NN Christchurch School of Medicine ZZZ NN NNNN Christchurch, New Zealand ZZZZZZZ Phone (64-3)364-0880 Fax (64-3)364-0750
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