Structural (Translocation) Heterozygosity Over Three Subsequent Generations in Man
- 1 July 1965
- journal article
- case report
- Published by Springer Nature in Nature
- Vol. 207 (4995) , 374-376
- https://doi.org/10.1038/207374a0
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Familial Chromosome-2, 3 Translocation Ascertained through an Infant with Multiple MalformationsNew England Journal of Medicine, 1964
- A 4–5/21–22 Chromosomal Translocation Associated with Multiple Congenital Anomalies1Acta Paediatrica, 1964
- PARTIAL ANEUPLOIDY A THIRD MODE OF INHERITANCE OF HUMAN DISEASEThe Lancet, 1964
- An Aberrant Autosome (13–15) in a Human Female and Her Father, both Apparently NormalCytogenetic and Genome Research, 1963
- Structural heterozygosis in man: analysis of two familiesAnnals of Human Genetics, 1962
- Familial transmission of a translocation between two chromosomes of the 13?15 group (Denver classification)Annals of Human Genetics, 1962
- A Familial Chromosome Abnormality Associated with Repeated AbortionsCytogenetic and Genome Research, 1962
- CHROMOSOME ANALYSIS FROM SMALL VOLUMES OF BLOODThe Lancet, 1961
- CHROMOSOMAL TRANSLOCATIONS IN MONGOLISM AND IN NORMAL RELATIVESThe Lancet, 1960
- CHROMOSOMAL ABNORMALITIES IN FATHER AND MONGOL CHILDThe Lancet, 1960