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virtual library in human genetics and molecular biology

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
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The papers listed above will appear in the 1995 review issue,
which is shortly to be printed. Copies are scheduled for
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