Human Chromosomal Heteromorphisms: Nature and Clinical Significance
- 1 January 1980
- book chapter
- Published by Elsevier
- Vol. 62, 361-383
- https://doi.org/10.1016/s0074-7696(08)61903-8
Abstract
No abstract availableThis publication has 83 references indexed in Scilit:
- The fluorescence pattern of a human Yq+ chromosomeHereditas, 2009
- Trisomy 21 in man due to maternal non-disjunction during the first meiotic divisionHereditas, 2009
- Fluorescent chromosome polymorphisms: frequencies and segregations in a Dutch populationClinical Genetics, 2008
- Trisomy 21 in a child due to paternal nondisjunction as determined by RFA techniqueJournal of Human Genetics, 1978
- Chromosome polymorphism in a human newborn populationCytogenetic and Genome Research, 1975
- SATELLITE STAINING OF HUMAN CHROMOSOMESThe Lancet, 1974
- Microfluorometric detection of asymmetry in the centromeric region of mouse chromosomesExperimental Cell Research, 1974
- New selective Giemsa technique for human chromosomes, Cd stainingNature, 1974
- ORIGIN OF EXTRA CHROMOSOME IN TRISOMY 21The Lancet, 1973
- The nature and inheritance of an elongated secondary constriction on chromosome 9 of manCytogenetic and Genome Research, 1973