What people are saying - Write a review
We haven't found any reviews in the usual places.
A Guide to Use of MIM
Appendices to the Foreword
B The Human Gene Map
3 other sections not shown
Other editions - View all
5-prime abnormalities Abstract Acad achondroplasia adenosine deaminase affected albumin alcohol allele alpha alpha-l-antitrypsin Alzheimer disease amino acid amino acid sequence amyloid amyloidosis analysis aniridia antibody antigen antithrombin APOB apoE apolipoprotein assigned associated autosomal dominant beta Biochem Biol blood group carcinoma cataract cDNA cDNA clones Cell Genet cell line chro chromosome 21 Clin clinical codon congenital Cytogenet defect deficiency dehydrogenase deletion demonstrated described disorder distal dominant inheritance dysplasia encoding enzyme erythrocyte exon frequency gene Genomics glycophorin hereditary homologous human chromosome identified inhibitor kinase kindred linkage lipoprotein liver located loci locus lod score males mapping markers molecular mosome mouse chromosome mRNA muscle mutation Neurol normal nucleotide patients peptide persons phenotype plasma polymorphism probe Proc protein receptor recessive recombination red cell region reported RFLP serum showed somatic cell hybrids structure studies subunit suggested syndrome translocation tumor variant X-linked