Clinical Genetics

Glaucoma genetics, present and future
pp. 71-79(9)
Authors: Friedman, James S; Walter, Michael A

Fetal gene therapy - a focus on prevention versus convention.
pp. 80-80(1)
Author: Lewis, Me Suzanne

Intra-amniotic viral gene transfer highlights the potential for in utero molecular therapies
pp. 80-81(2)
Author: Lewis, Me Suzanne

The tools of gene therapy can create new insights in developmental biology
pp. 81-82(2)
Author: Lewis, Me Suzanne

Fetal gene therapy confers stable gene expression, germline and widespread somatic cell transfection
pp. 82-84(3)
Author: Lewis, Me Suzanne

Genetic landmarks through philately - porphyria and its effect on world history
pp. 85-87(3)
Authors: Chudley, Albert E; Haworth, James C

Evaluation of the facioscapulohumeral muscular dystrophy (FSHD1) phenotype in correlation to the concurrence of 4q35 and 10q26 fragments
pp. 88-94(7)
Authors: Köhler, Jutta; Röhrig, Dorothee; Bathke, Klaus D; Koch, Manuela C

Pattern of central nervous system anomalies in a population with a high rate of consanguineous marriages
pp. 95-102(8)
Authors: Al-Gazali, Li; Sztriha, L; Dawodu, A; Bakir, M; Varghese, M; Varady, E; Scorer, J; Abdulrazzaq, Ym; Bener, A; Padmanabhan, R

Antibody deficiency, growth retardation, spondyloepiphyseal dysplasia and retinal dystrophy: a novel syndrome
pp. 103-109(7)
Author: Roifman, Chaim M

Novel exon skipping mutation in the fibrillin-1 gene: Two `hot spots' for the neonatal Marfan syndrome
pp. 110-117(8)
Authors: Booms, Patrick; Cisler, Jason; Mathews, Kurt R.; Godfrey, Maurice; Tiecke, Frank; Kaufmann, Ursula C.; Vetter, Ulrich; Hagemeier, Christian; Robinson, Peter N.

Alternative splicing of exon 37 of FBN1 deletes part of an `eight-cysteine' domain resulting in the Marfan syndrome
pp. 118-121(4)
Authors: McGrory, Joel; Cole, William G

Centromere-telomere (12;8p) fusion, telomeric 12q translocation, and i(12p) trisomy
pp. 122-126(5)
Authors: Rivera, Horacio; Vásquez, Ana Isabel; Perea, Francisco J

Deletion of chromosome 4p detected by FISH in a girl with normal high resolution karyotype
pp. 127-129(3)

Mutations associated with very late-onset metachromatic leukodystrophy
pp. 130-130(1)

Preaxial polydactyly in an infant with Down's syndrome
pp. 131-132(2)

Correspondence
pp. 133-134(2)

Obituary
pp. 135-136(2)