Molecular and Cytogenetic Evidence for the Location of Tdy and Hya on the Mouse Y Chromosome Short Arm

Autor: Roberts, C., Weith, A., Passage, E., Michot, J. L., Mattei, M. G., Bishop, C. E.

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America, 1988 Sep 01. 85(17), 6446-6449.

Externí odkaz: https://www.jstor.org/stable/32036

Organization of the X and Y chromosomes in human, chimpanzee and mouse pachytene nuclei using molecular cytogenetics and three-dimensional confocal analyses

Autor: Metzler-Guillemain, C., Usson, Yves, Mignon, C., Depetris, D., Dubreuil, G., Guichaoua, M. R., Mattei, M. G.

Publikováno v: Chromosome Research
Chromosome Research, Springer Verlag, 2000, 8 (7), pp.571-84. ⟨10.1023/A:1009277722579⟩
Chromosome Research, 2000, 8 (7), pp.571-84. ⟨10.1023/A:1009277722579⟩

We used multicolour fluorescence in-situ hybridization on air-dried pachytene nuclei to analyse the structural and functional domains of the sex vesicle (SV) in human, chimpanzee and mouse. The same technology associated with 3-dimensional analysis w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0ff373e3b577366fe7c5c1b6e86a4d31
https://hal.archives-ouvertes.fr/hal-00192539

A novel mechanism for thalassaemia intermedia.

Autor: Badens, C, Mattei, M G, Imbert, A M, Lapouméroulie, C, Martini, N, Michel, G, Lena-Russo, D, Lapouméroulie, C (AUTHOR)

Publikováno v: Lancet. 1/12/2002, Vol. 359 Issue 9301, p132-133. 2p. 1 Color Photograph, 1 Diagram.

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

Autor: Machey, N., Saut, N., Longepieci, G., Terriou, P., Navarro, A., Levy, N., Guichaoua, M., Metzler-Guillemain, C., Collignon, P., Frances, A.-M., Belougne, J., Clemente, E., Chiaroni, J., Chevillard, C., Durand, C., Ducourneau, A., Pech, N., McElreavey, K., Mattei, M.-G., Mitchell, M. J.

Publikováno v: Journal of Medical Genetics; Nov2004, Vol. 41 Issue 11, p814-825, 11p, 1 Black and White Photograph, 5 Diagrams, 6 Charts

Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations.

Autor: Luciani, J.J., de Mas, P., Depetris, D., Mignon-Ravix, C., Bottani, A., Prieur, M., Jonveaux, P., Philippe, A., Bourrouillou, G., de Martinville, B., Delobel, B., Vallee, L., Croquette, M.-F., Mattei, M.-G.

Publikováno v: Journal of Medical Genetics; Sep2003, Vol. 40 Issue 9, p690-696, 7p, 1 Color Photograph, 2 Diagrams, 1 Chart