Introductory comments special section: Trisomy 18
Neonatal management of trisomy 18: Clinical details of 24 patients receiving intensive treatment
Clinical characteristics and survival of trisomy 18 in a medical center in Taipei, 1988–2004
Survival with trisomy 18—data from Switzerland
Aplasia and duplication of the thumb and facial clefts associated with fetal trisomy 18
Regarding trisomy 18
Trisomy 18 in a second 20-year-old woman
Behavioral and temperamental features of children with Costello syndrome
A prospective study of PHACE syndrome in infantile hemangiomas: Demographic features, clinical findings, and complications
Maternal polymorphisms 677C-T and 1298A-C of MTHFR, and 66A-G MTRR genes: Is there any relationship between polymorphisms of the folate pathway, maternal homocysteine levels, and the risk for having a child with Down syndrome?
Prenatal diagnosis of hypochondroplasia: Report of two cases
Fumarase deficiency caused by homozygous P131R mutation and paternal partial isodisomy of chromosome 1
Can we exclude the TXNIP gene as a candidate gene for familial combined hyperlipidemia?
Familial Klippel–Feil anomaly and t(5;8)(q35.1;p21.1) translocation
del5p/dup5q in a ‘cri du chat’ patient without parental chromosomal rearrangement
A novel duplication/insertion mutation of NEFL in a patient with Charcot-Marie-Tooth disease
Prader–Willi syndrome: Development and manifestations. By Joyce Whittington and Tony Holland
Association of Adams–Oliver syndrome and hepatoportal sclerosis: An additional case
Clarification of data reported in “Cleidocranial Dysplasia: Molecular Genetic Analysis and Phenotypic-Based Description of a Middle European Patient Group” (AJMG 139A:78–85)
Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): A possible locus for Fryns syndrome (Am J Med Genet 140A:17–23, 2006)