N. Saut

Common variants in the thrombomodulin gene as a risk for myocardial infarction in the North of Europe (HIFMECH study) (2004)

Konstantoulas, C.J., Hawe, E., Saut, N., Yudkin, J.S., Diminno, G., Margaglione, M., ...

The mouse Y chromosome interval necessary for spermatogonial proliferation is gene dense with syntenic homology to the human AZFa region (1998)

Mazeyrat, S, Saut, N, Sargent, CA, Grimmond, S, Longepied, G, Ehrmann, IE, ...

The critical region of overlap defining the AZFa male infertility interval of proximal Yq contains three transcribed sequences

Sargent, C., Boucher, C., Kirsch, S., Brown, G., Weiss, B., Trundley, A., ...

The position of deletion breakpoints in a series of four AZFa male infertility patients has been refined using new markers derived from BAC clone DNA sequence covering the AZFa male infertility...

Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility

Machev, N, Saut, N, Longepied, G, Terriou, P, Navarro, A, Levy, N, ...

Background: Complete deletion of the complete AZFc interval of the Y chromosome is the most common known genetic cause of human male infertility. Two partial AZFc deletions (gr/gr and b1/b3) that...