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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
Executive Editors:-
K E Davies, Oxford, UK
Huntington F Willard, Cleveland, OH, USA

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
     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
     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.


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

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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