Growing interest in Turner syndrome

This publication has 9 references indexed in Scilit:

• Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
  Nature Genetics, 1997
• Whither Down syndrome critical regions?
  Human Genetics, 1997
• The molecular basis of hypodactyly (Hd): a deletion in Hoxa13 leads to arrest of digital arch formation
  Nature Genetics, 1996
• Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
  Nature, 1995
• Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
  Nature, 1994
• Homologous ribosomal protein genes on the human X and Y chromosomes: Escape from X inactivation and possible implications for turner syndrome
  Cell, 1990
• Karyotype-phenotype Correlations in Gonadal Dysgenesis and Their Bearing on the Pathogenesis of Malformations
  Journal of Medical Genetics, 1965
• A SEX-CHROMOSOME ANOMALY IN A CASE OF GONADAL DYSGENESIS (TURNER'S SYNDROME)
  The Lancet, 1959
• A SYNDROME OF INFANTILISM, CONGENITAL WEBBED NECK, AND CUBITUS VALGUS1
  Endocrinology, 1938