Abnormal X chromosomes in man: origin, behavior and effects - PubMed (original) (raw)
- PMID: 4475024
- DOI: 10.1007/BF00281002
Abnormal X chromosomes in man: origin, behavior and effects
E Therman et al. Humangenetik. 1974.
No abstract available
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References
- Ann Genet. 1970 Dec;13(4):245-8 - PubMed
- Humangenetik. 1973;20(2):163-6 - PubMed
- Am J Hum Genet. 1965 Sep;17:377-83 - PubMed
- Proc Natl Acad Sci U S A. 1972 Jan;69(1):69-73 - PubMed
- Am J Hum Genet. 1971 Jul;23(4):410-8 - PubMed