Localization of the Gene for Congenital Dyserythropoietic Anemia Type I to a <1-cM Interval on Chromosome 15q15.1-15.3

This publication has 20 references indexed in Scilit:

• Exclusion of Three Candidate Genes as Determinants of Congenital Dyserythropoietic Anemia Type II (CDA-II)
  Blood, 1997
• Localization of the Congenital Dyserythropoietic Anemia II Locus to Chromosome 20q11.2 by Genomewide Search
  American Journal of Human Genetics, 1997
• A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene
  Human Molecular Genetics, 1995
• Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
  Cell, 1995
• Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population
  Nature Genetics, 1995
• Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25
  Human Molecular Genetics, 1995
• Incompletely processed N‐glycans of serum glycoproteins in congenital dyserythropoietic anaemia type II (HEMPAS)
  British Journal of Haematology, 1992
• Organization of the gene for human erythrocyte membrane protein 4.2: structural similarities with the gene for the a subunit of factor XIII.
  Proceedings of the National Academy of Sciences, 1991
• Homozygosity Mapping: A Way to Map Human Recessive Traits with the DNA of Inbred Children
  Science, 1987
• Construction of Human Gene Libraries from Small Amounts cf Peripheral Blood: Analysis of β-Like Globin Genes
  Hemoglobin, 1981