Monosomy for 21pter-q21: Case report and assignment of a DNA clone (Fr8-77) to the deleted segment

Author:

Abe Kyohko,Deng Han-Xiang,Harada Naoki,Yoshiura Koh-ichiro,Oh-hira Takahiko,Nikawa Norio

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical)

Reference23 articles.

1. David, K.K., Hsu, L.Y.F., Cristian, S. and Hirschhorn, K. 1977. “Monosomy” re-evaluated.Pediatr. Res. 11:454.

2. de Grouchy, J. and Turleau, C. 1984. Chromosome 21. InClinical Atlas of Human Chromosomes, 2nd Ed., John Wiley & Sons, New York, pp. 336–359.

3. Dutrillaux, B., Jonasson, J., Lauren, K., Lejeune, J., Lindsten, J., Petersen, G.B. and Saldana-Garcia, P. 1973. An unbalanced 4q/21q translocation identified by the R but not by the G and Q chromosome banding techniques.Ann. Génét. 16:11–16.

4. Dziuba, P., Dziekanowska, D. and Hubner, H. 1976. A female infant with monosomy 21.Hum. Genet. 31:351–353.

5. Ferrante, E., Vignetti, P., Antonelli, M., Bruni, L., Bertasi, S. and Chessa, L. 1983. Partial monosomy for a 21 chromosome.Helv. Paediatr. Acta 38:73–80.

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