Significance of chromosome 17ps+ in three generations of a family.
Open Access
- 1 June 1970
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 7 (2) , 142-147
- https://doi.org/10.1136/jmg.7.2.142
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- HERITABLE MORPHOLOGICAL DIFFERENCE BETWEEN THE TWO CHROMOSOMES NO. 16 IN HUMANSHereditas, 2009
- A HOMOZYGOUS CHROMOSOMAL VARIANTThe Lancet, 1969
- Probable assignment of the Duffy blood group locus to chromosome 1 in man.Proceedings of the National Academy of Sciences, 1968
- Chromosomal Abnormalities and Congenital Heart DiseaseCirculation, 1967
- THE CRI-DU-CHAT SYNDROME WITH AN APPARENTLY NORMAL KARYOTYPEThe Lancet, 1967
- Familial Congenital Heart DiseaseCirculation, 1966
- The Sites and Relative Frequencies of Secondary Constrictions in Human Somatic ChromosomesCytogenetic and Genome Research, 1962
- OBSERVATIONS ON THE SATELLITED HUMAN CHROMOSOMESThe Lancet, 1961
- Chromosome preparations of leukocytes cultured from human peripheral bloodExperimental Cell Research, 1960
- THE SOMATIC CHROMOSOMAL CONSTITUTION OF SOME HUMAN SUBJECTS WITH GENETIC DEFECTSProceedings of the National Academy of Sciences, 1959