Clinical Genetics

HRAS and the Costello syndrome
pp. 101-108(8)
Author: Rauen,

Gene discovery in craniofacial development and disease - cashing in your chips
pp. 109-119(11)
Authors: Handrigan,; Buchtová,; Richman,

Young people's experiences of growing up in a family affected by Huntington's disease
pp. 120-129(10)
Authors: Forrest Keenan,; Miedzybrodzka,; van Teijlingen,; McKee,; Simpson,

Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC
pp. 130-139(10)
Authors: Stella,; Surdo,; Lastella,; Barana,; Oliani,; Tibiletti,; Viel,; Natale,; Piepoli,; Marra,; Guanti,

A comparison of community, clinician, and patient preferences for naming a cancer-related mutation
pp. 140-147(8)
Authors: Wakefield,; Meiser,; Homewood,; Barlow-Stewart,; Tucker,

A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1
pp. 148-152(5)
Authors: Kitajiri,; Makishima,; Friedman,; Griffith,

A survey of preventive measures among BRCA1 mutation carriers from Poland
pp. 153-157(5)
Authors: Gronwald,; Byrski,; Huzarski,; Cybulski,; Stawicka,; Szwiec,; Dębniak,; Tulman,; Sun,; Oszurek,; Lubinski,; Narod,

Effectiveness of thecrcaproprogram in identifying patients suspected for HNPCC
pp. 158-164(7)
Authors: Bianchi,; Galizia,; Bracci,; Belvederesi,; Catalani,; Loretelli,; Giorgetti,; Ferretti,; Bearzi,; Porfiri,; Cellerino,

Contribution of BRCA1 and BRCA2 germline mutations to the incidence of early-onset breast cancer in Cyprus
pp. 165-170(6)
Authors: Loizidou,; Marcou,; Anastasiadou,; Newbold,; Hadjisavvas,; Kyriacou,

A possible bichromatid mutation in a male gamete giving rise to a female mosaic for two different mutations in the X-linked gene WAS
pp. 171-176(6)
Authors: Dobbs,; Yang,; Farmer,; Howard,; Conley,

1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features
pp. 177-182(6)
Authors: Alberti,; Romano,; Falco,; Calì,; Schinocca,; Galesi,; Spalletta,; Di Benedetto,; Fichera,

Novel LMNA mutations seen in patients with familial partial lipodystrophy subtype 2 (FPLD2; MIM 151660)
pp. 183-186(4)

Three children with Milroy disease and de novo mutations in VEGFR3
pp. 187-189(3)

Novel germline and somatic mutations of the MSH2 gene in hereditary non-polyposis colorectal cancer
pp. 190-192(3)

Corrigendum
pp. 193-193(1)

Corrigendum
pp. 194-194(1)