Familial pericentric inversion of chromosome 1 (p34q23) and male infertility with stage specific spermatogenic arrest.

Author:

Meschede D,Froster U G,Bergmann M,Nieschlag E

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference9 articles.

1. Cytogenetic studies in male infertility: a review;M, De Braekeleer; TN, Dao;Hum Reprod,1991

2. Familial inv(I)(p36.3q12) associated with sterility;Barros, A.; Tavares, M.C.; Gomes, M.P.; Tavares, M.P.;Med Genet,1986

3. Electron microscopic investigations of synaptonemal complexes in an infertile male carrier of a pericentric inversion inv(1)(p32q42);Batanian, J.; Hulten, M.A.;Hum Genet,1987

4. Pericentric inversion in human chromosome 1 and the risk for male sterility;Chandley, A.C.; McBeath, S.; Speed, R.M.; Yorston, L.; Hargreave, T.B.;Med Genet,1987

5. Synapsis and synaptic adjustment in an infertile human male heterozygous for a pericentric inversion in chromosome 1,1986

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