References
Chamla Y, Roumy M, Lassègues M, Battin J (1980) Altered sensitivity to colchicine and PHA in human cultured cells. Hum Genet 53:249–253
Fitzgerald PH (1975) A mechanism of X chromosome aneuploidy in lymphocytes of aging women. Humangenetik 28:153–158
Gabarrón J, Jimenez A, Glover G (1986) Premature centromere division dominantly inherited in a subfertile family. Cytogenet Cell Genet 43:69–71
German J (1979) Robert's syndrome. I. Cytological evidence for a disturbance in chromatid pairing. Clin Genet 16:441–447
Madan K, Lindhout D, Palan B (1987) Premature centromere division (PCD): a dominantly inherited cytogenetic anomaly. Hum Genet 77:193–196
Mehés K, Bajnóczy K (1981) Early centromere division: analysis of G-banded human chromosomes and family investigations. Clin Genet 19:515
Rudd N, Teshima IE, Martin R, Sisken JE, Weksberg R (1983) A dominantly inherited cytogenetic anomaly: a possible cell division mutant. Hum Genet 65:117–121
Scheres JMJC, Hustinx TWJ, Madan K, Beltman JD, Lindhout D (1986) A mitotic mutant causing non-disjunction in man. In: 7th International Congress of Human Genetics, Berlin 1986, p 163 (abstr).
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Madan, K. Reply to the letter by Y. Chamla, C-anaphases rediscovered. Hum Genet 79, 94 (1988). https://doi.org/10.1007/BF00291723
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DOI: https://doi.org/10.1007/BF00291723