Deleted Chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genes

This publication has 47 references indexed in Scilit:

• The Human Type 2 Cystatin Gene Family Consists of Eight to Nine Members, with at Least Seven Genes Clustered at a Single Locus on Human Chromosome 20
  DNA and Cell Biology, 1994
• Phosphoenolpyruvate Carboxykinase (GTP): Characterization of the Human PCK1 Gene and Localization Distal to MODY on Chromosome 20
  Genomics, 1993
• Cystatin C (CST3), the Candidate Gene for Hereditary Cystatin C Amyloid Angiopathy (HCCAA), and Other Members of the Cystatin Gene Family Are Clustered on Chromosome 20p11.2
  Genomics, 1993
• Localization of the human cystatin D gene (CST5) to chromosome 20p11.21 by in situ hybridization
  Cytogenetic and Genome Research, 1993
• PAX1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in Situ hybridization (ISH and FISH)
  Genomics, 1992
• A one-step efficient and specific non-radioactive non-fluorescent method for in situ hybridization of banded chromosomes
  Chromosoma, 1990
• The human cystatin C gene (CST3) is a member of the cystatin gene family which is localized on chromosome 20
  Biochemical and Biophysical Research Communications, 1989
• Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): Review of 80 cases
  The Journal of Pediatrics, 1987
• Contiguous gene syndromes: A component of recognizable syndromes
  The Journal of Pediatrics, 1986
• Syndromatic hepatic ductular hypoplasia (arteriohepatic dysplasia)
  Digestive Diseases and Sciences, 1981