Anomalies des autosomes et infertilité masculine

Author:

Rumpler Yves,Gabrel-Robez Odette

Publisher

Springer Science and Business Media LLC

Subject

Urology,Reproductive Medicine

Reference38 articles.

1. AN EUROPEAN COLLABORATIVE STUDY.: The meiotic pairing behaviour in human spermatocytes carrier of chromosome anomalies and their repercussions on reproductive fitness. I. Inversions and Insertion. Prepared by O Gabriel Robez and Y. Rumpler. Ann. Génét, in press.

2. BATANIAN J., HULTEN M.A.: Electron microscopic investigations of synaptonemal complexes in an infertile male carrier of a pericentric inversion inv (1) (p32; q42). Regular loop formation but defective synapsis including a possible interchromosomal effect. Him. Genet., 1987, 76: 81–86.

3. CHANDLEY A.C., SPEED R.M., MCBEATH S., HARGREAVE T.B.: A human 9j20 reciprocal translocation associated with male infertility analyzed at prophase and metaphase I of meiosis. Cytogenet. Cell Genet., 1986, 41: 145–153.

4. CHANDLEY A.C., MCBEATH S., SPEED R.M., YORSTON L., HARGREAVE T.B.: Pericentric inversion in human chromosome 1 and the risk for male sterility. J. Med. Genet., 1987, 24: 325–334.

5. DUTRILLAUX B., GUEGEN J.: Etude méiotique et mitotique dans un cas de translocation t (5;Y). Hum. Genet., 1971, 27: 241–245.

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