Human Molecular Genetics

REVIEWS:

Jean-Michel Claverie

Computational methods for theidentification of differential and coordinated gene expression
Hum. Mol. Genet. 1999 8: 1821-1832; doi:10.1093/hmg/8.10.1821 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Jamel Chelly

Breakthroughs in molecular andcellular mechanisms underlying X-linked mental retardation
Hum. Mol. Genet. 1999 8: 1833-1838; doi:10.1093/hmg/8.10.1833 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Francesca Lazner, Maxine Gowen, Durda Pavasovic, and Ismail Kola

Osteopetrosis and osteoporosis:two sides of the same coin
Hum. Mol. Genet. 1999 8: 1839-1846; doi:10.1093/hmg/8.10.1839 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Glenn E. Morris and Sushila Manilal

Heart to heart: from nuclearproteins to Emery–Dreifuss muscular dystrophy
Hum. Mol. Genet. 1999 8: 1847-1851; doi:10.1093/hmg/8.10.1847 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Brian C. Schutte and Jeffrey C. Murray

The many faces and factors oforofacial clefts
Hum. Mol. Genet. 1999 8: 1853-1859; doi:10.1093/hmg/8.10.1853 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Peter C. Harris

Autosomal dominant polycystickidney disease: clues to pathogenesis
Hum. Mol. Genet. 1999 8: 1861-1866; doi:10.1093/hmg/8.10.1861 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Mellissa R. W. Mann and MarisaS. Bartolomei

Towards a molecular understandingof Prader–Willi and Angelman syndromes
Hum. Mol. Genet. 1999 8: 1867-1873; doi:10.1093/hmg/8.10.1867 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Katharine M. D. Bushby

The limb-girdle muscular dystrophies—multiple genes,multiple mechanisms
Hum. Mol. Genet. 1999 8: 1875-1882; doi:10.1093/hmg/8.10.1875 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Lorraine A. Everett and EricD. Green

A family of mammalian anion transportersand their involvement in human genetic diseases
Hum. Mol. Genet. 1999 8: 1883-1891; doi:10.1093/hmg/8.10.1883 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Pamela A. Frischmeyer and HarryC. Dietz

Nonsense-mediated mRNA decayin health and disease
Hum. Mol. Genet. 1999 8: 1893-1900; doi:10.1093/hmg/8.10.1893 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Matt Farrer, Katrina Gwinn-Hardy, Mike Hutton, and John Hardy

The genetics of disorders withsynuclein pathology and parkinsonism
Hum. Mol. Genet. 1999 8: 1901-1905; doi:10.1093/hmg/8.10.1901 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Colin F. Fletcher and WayneN. Frankel

Ataxic mouse mutantsand molecular mechanisms of absence epilepsy
Hum. Mol. Genet. 1999 8: 1907-1912; doi:10.1093/hmg/8.10.1907 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Leena Peltonen, Anu Jalanko, and Teppo Varilo

Molecular genetics of the Finnishdisease heritage
Hum. Mol. Genet. 1999 8: 1913-1923; doi:10.1093/hmg/8.10.1913 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

George R. Stark and AndreiV. Gudkov

Forward genetics in mammaliancells: functional approaches to gene discovery
Hum. Mol. Genet. 1999 8: 1925-1938; doi:10.1093/hmg/8.10.1925 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Mary Carrington, Michael Dean, Maureen P. Martin, and StephenJ. O’Brien

Genetics of HIV-1infection: chemokine receptor CCR5 polymorphism and its consequences
Hum. Mol. Genet. 1999 8: 1939-1945; doi:10.1093/hmg/8.10.1939 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Uta Francke

Williams–Beuren syndrome:genes and mechanisms
Hum. Mol. Genet. 1999 8: 1947-1954; doi:10.1093/hmg/8.10.1947 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Monica J. Justice, JaniceK. Noveroske, JohnS. Weber, Binhai Zheng, and Allan Bradley

Mouse ENU Mutagenesis
Hum. Mol. Genet. 1999 8: 1955-1963; doi:10.1093/hmg/8.10.1955 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

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