• A clinical follow-up of British patients with FG syndrome
• A gene for FG syndrome maps in the Xq12-q21.31 region
• An autosomal recessive mental retardation syndrome with hepatic fibrosis and renal cysts
• FG syndrome
• High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with Cancer
• Kivlin syndrome and Peters'-Plus syndrome: are they the same disorder?
• Multiple pterygium syndrome: evolution of the phenotype
• Nosology of Smith-Lemli-Opitz syndrome
• Parietal foramina in Saethre-Chotzen syndrome
• Rapadilino syndrome--a non-Finnish case
• Severe Silver-Russell syndrome
• Sorsby syndrome: a report on further generations of the original family
• The FG syndrome: 7 new cases
• The Nager acrofacial dysostosis syndrome with the tetralogy of Fallot
• X linked mental retardation: a family with a separate syndrome?