A MONGOL WITH A 21:22 TYPE CHROMOSOMAL TRANSLOCATION
- 28 June 2008
- journal article
- Published by Wiley in Journal of Intellectual Disability Research
- Vol. 7 (2) , 84-89
- https://doi.org/10.1111/j.1365-2788.1963.tb00787.x
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
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- PATERNAL AGE IN MONGOLISMThe Lancet, 1962
- PERICENTRIC INVERSION OF CHROMOSOME 21 A POSSIBLE FURTHER CYTOGENETIC MECHANISM IN MONGOLISMThe Lancet, 1962
- Familial MongolismCytogenetic and Genome Research, 1962
- Langdon Down Anomaly (Mongolism) with 21/21 Translocation and Klinefelter’s Syndrome in the same SibshipCytogenetic and Genome Research, 1962
- CHROMOSOME STUDIES IN DETECTION OF PARENTS WITH HIGH RISK OF SECOND CHILD WITH DOWN'S SYNDROMEThe Lancet, 1961
- CHROMOSOMAL TRANSLOCATIONS IN MONGOLISM AND IN NORMAL RELATIVESThe Lancet, 1960
- CHROMOSOMAL ABNORMALITIES IN FATHER AND MONGOL CHILDThe Lancet, 1960