Assignment of the Locus for Congenital Lactase Deficiency to 2q21, in the Vicinity of but Separate from the Lactase-Phlorizin Hydrolase Gene

This publication has 22 references indexed in Scilit:

• The Finnish population structure A genetic and genealogical study
  Hereditas, 2009
• Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus.
  Genome Research, 1996
• A comprehensive genetic map of the human genome based on 5,264 microsatellites
  Nature, 1996
• A new bacteriophage P1–derived vector for the propagation of large human DNA fragments
  Nature Genetics, 1994
• Radiation Hybrid Mapping: A Somatic Cell Genetic Method for Constructing High-Resolution Maps of Mammalian Chromosomes
  Science, 1990
• The human lactase‐phlorizin hydrolase gene is located on chromosome 2
  FEBS Letters, 1988
• Blot hybridisation analysis of genomic DNA.
  Journal of Medical Genetics, 1984
• Congenital lactase deficiency. A clinical study on 16 patients.
  Archives of Disease in Childhood, 1983
• LACTOSE MALABSORPTION IN FINNISH CHILDREN OF SCHOOL AGE
  Acta Paediatrica, 1972
• DEFECTIVE LACTOSE ABSORPTION CAUSING MALNUTRITION IN INFANCY
  The Lancet, 1959