The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(qh?,RHG,GAG,CBG)

Author:

Donti E.,Venti G.,Bocchini V.,Rosi Gabriella,Armellini R.,Trabalza N.,Bettini G.,Pimpinelli F.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference33 articles.

1. Aula, P., von Koskull, H.: Distribution of spontaneous chromosome breaks in human chromosomes. Humangenetik 32, 143?148 (1976)

2. Aym�, S., Mattei, J. F., Mattei, M. G., Aurran, Y., Giraud, F.: Non-random distribution of chromosome breaks in cultured lymphocytes of normal subjects. Humangenetik 31, 161?175 (1976)

3. Biederman, B., Bowen, P.: Balanced translocations involving chromosome 12: report of a case and possible evidence for position effect. Ann. Genet. (Paris) 19, 257?260 (1976)

4. Br�gger, A.: Is the chromatid gap a folding defect due to protein change? Evidence from mercaptoethanol treatment of human lymphocyte chromosomes. Hereditas 80, 131?136 (1975)

5. B�hler, E. M., Luchsinger, U., B�hler, U. K., Mehes, K., Stalder, G. R.: Non-condensation of one segment of a chromosome No. 2 in a male with an otherwise normal karyotype (and severe hypospadias). Humangenetik 9, 97?104 (1970)

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