A fetus with recombinant of chromosome 8 inherited from her carrier father

Author:

Fujimoto Atsuko,Towner Joseph W.,Turkel Susan B.,Wilson Miriam G.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference33 articles.

1. Allderdice, P. W., Browne, N., Murphy, D. P.: Chromosome 3 duplication q21?qter deletion p25?pter syndrome in children of carriers of pericentric inversion inv(3)(p25q21). Am. J. Hum. Genet. 27, 699?718 (1975)

2. Atkins, L., Holmes, L. B., Riccardi, V. M.: Trisomy 8. J. Pediatr. 84, 302?304 (1974)

3. Bou�, J., Taillemite, J. L., Hazael-Massieux, P., L�onard, C., Bou�, A.: Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families. Humangenetik 30, 217?224 (1975)

4. Chapelle, A. de la, Schr�der, J., Stenstrand, K., Fellman, J., Herva, R., Saarni, M., Anttolainen, I., Tallila, I., Tervila, L., Husa, L., Robson, E. B., Cook, P. J. L., Sanger, R.: Pericentric inversions of human chromosomes 9 and 10. Am. J. Hum. Genet. 26, 746?766 (1974)

5. Cohen, M. M., Davidson, R. G.: An inherited pericentric chromosomal inversion (46,inv(3) (p-q+)) associated with skeletal anomalies. J. Pediatr. 79, 456?462 (1971)

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