The CEPH consortium linkage map of human chromosome 2

This publication has 14 references indexed in Scilit:

• Centre d'Etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genome
  Published by Elsevier ,2004
• An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
  Nature, 1992
• The CEPH consortium linkage map of human chromosome 1
  Genomics, 1991
• Structure and polymorphism of human telomere-associated DNA
  Cell, 1990
• Possible locus for polycystic kidney disease on chromosome 2
  The Lancet, 1990
• Standard maps of chromosome 10
  Annals of Human Genetics, 1990
• Twenty loci form a continuous linkage map of markers for human chromosome 2
  Genomics, 1989
• Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3)
  American Journal of Medical Genetics, 1989
• Holoprosencephaly: Association with interstitial deletion of 2p and review of the cytogenetic literature
  American Journal of Medical Genetics, 1988
• A genetic linkage map of the human genome
  Cell, 1987