Clinical Genetics

Dyskeratosis congenita: a genetic disorder of many faces
pp. 103-112(10)
Authors: Kirwan,; Dokal,

Synpolydactyly: clinical and molecular advances
pp. 113-120(8)
Authors: Malik,; Grzeschik,

Predictors of psychological distress among individuals with a strong family history of malignant melanoma
pp. 121-131(11)
Authors: Kasparian,; Meiser,; Butow,; Simpson,; Mann,

Cultural enhancement of a clinical service to meet the needs of indigenous people; genetic service development in response to issues for New Zealand Maori
pp. 132-138(7)
Authors: Port,; Arnold,; Kerr,; Gravish,; Winship,

Two new patients bearing mutations in the fukutin gene confirm the relevance of this gene in Walker-Warburg syndrome
pp. 139-145(7)
Authors: Cotarelo,; Valero,; Prados,; Peña,; Rodríguez,; Fano,; Marco,; Martínez-Frías,; Cruces,

Mutations in the familial Mediterranean fever gene of patients with IgA nephropathy and other forms of glomerulonephritis
pp. 146-151(6)
Authors: Kukuy,; Kopolovic,; Blau,; Ben-David,; Lotan,; Shaked,; Shinar,; Dinour,; Langevitz,; Livneh,

Familial Mediterranean Fever in Crete: a genetic and structural biological approach in a population of `intermediate risk'
pp. 152-159(8)
Authors: Fragouli,; Eliopoulos,; Petraki,; Sidiropoulos,; Aksentijevich,; Galanakis,; Kritikos,; Repa,; Fragiadakis,; Boumpas,; Goulielmos,

Familial 22q11.2 duplication: a three-generation family with a 3-Mb duplication and a familial 1.5-Mb duplication
pp. 160-164(5)
Authors: Yu,; Cox,; Friend,; Smith,; Buchheim,; Bain,; Liebelt,; Thompson,; Bratkovic,

Pediatric restrictive cardiomyopathy associated with a mutation in β-myosin heavy chain
pp. 165-170(6)
Authors: Ware,; Quinn,; Ballard,; Miller,; Uzark,; Spicer,

Novel mutations of the ferroportin gene (SLC40A1): analysis of 56 consecutive patients with unexplained iron overload
pp. 171-178(8)
Authors: Pelucchi,; Mariani,; Salvioni,; Bonfadini,; Riva,; Bertola,; Trombini,; Piperno,

Novel rare mutations and promoter haplotypes in ABCA1 contribute to low-HDL-C levels
pp. 179-184(6)
Authors: Slatter,; Jones,; Williams,; van Rij,; McCormick,

High frequency of T130I mutation of HNF4A gene in Mexican patients with early-onset type 2 diabetes
pp. 185-187(3)

Restoring reproductive confidence in families with X-linked mental retardation by finding the causal mutation
pp. 188-190(3)

Perinatal lethal Gaucher's disease without prenatal complications
pp. 191-195(5)

Corrigendum
pp. 196-196(1)