On the X Chromosome of Man |
Contents
Introduction | 1 |
B Significance of dominance and | 17 |
Linkage data on the constitution of the X | 23 |
Copyright | |
4 other sections not shown
Common terms and phrases
abnormalities Acta active affected males allelism appears Arch associated autosomal autosomal dominant Barr body basis blood group brothers carrier cells cent chro chromatin chromo colleagues color blindness congenital consistent daughters defect deficiency demonstrated described determined disease disorder dominant doubly estimated et al evidence example expected fact factor father female Figure findings four frequency genes glucose-6-phosphate hemophilia hereditary heterozygous Human Genet indicated inheritance Kallmann syndrome Lancet least linkage linked loci locus mechanism mental method mosaic mosome mother mouse muscular dystrophy mutation Nature normal observed occur parents partial patient pattern pedigree phenotype possible present probably Proc proportion ratio recessive recombination relation relative reported result rickets separate sex chromosome sex-linked sons studies suggested tion traits Turner syndrome X chromosome X-linkage X-linked X-linked recessive X-linked traits