The 50th anniversary of the discovery of trisomy 21: The past, present, and future of research and treatment of Down syndrome von Mégarbané, André, Ravel, Aimé, Mircher, Clotilde, Sturtz, Franck, Grattau, Yann, Rethoré, Marie-Odile, Delabar, Jean-Maurice, Mobley, William C

Volltext

An ovarian dysgerminoma in Down syndrome. Hypothesis about the association von SATGÉ, D., HONORÉ, L., SASCO, A.J., VEKEMANS, M., CHOMPRET, A., RÉTHORÉ, M.‐O

Volltext

De novo complex chromosomal rearrangements (CCR) involving chromosome 1, 5, and 6 resulting in microdeletion for 6q14 in a female carrier with psychotic disorder von Lespinasse, James, Bugge, M., Réthoré, M.O., North, M.O., Lundsteen, C., Kirchhoff, M.

Volltext

Eleven new cases of del(9p) and features from 80 cases von Huret, J L, Leonard, C, Forestier, B, Rethoré, M O, Lejeune, J

Volltext

ETUDE DE LA DESCENDANCE DE SUJETS TRAITÉS PAR RADIOTHÉRAPIE PELVIENNE von Turpin, R., Lejeune, J., Rethore, M.-O.

Volltext

Differences in purine metabolism in patients with Down's syndrome von PEETERS, M. A., MEGARBANE, A., CATTANEO, F., RETHORE, M.-O., LEJEUNE, J.

Volltext

A 23-year-old woman with down syndrome, type 1 neurofibromatosis, and breast carcinoma von Satgé, Daniel, Sasco, Annie J., Goldgar, David, Vekemans, Michel, Réthoré, Marie-Odile

Volltext

Les dysmorphies liées aux aberrations chromosomiques autosomiques de l'enfant à l'adulte von RETHORE, M.-O

Volltext

Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene von ION, R, TELVI, L, CHAUSSAIN, J.-L, BARBET, J. P, NUNES, M, SAFAR, A, RETHORE, M.-O, FELLOUS, M, MCELREAVEY, K

Volltext

DNA polymorphism analysis in families with recurrence of free trisomy 21 von PANGALOS, C. G, CONOVER TALBOT, C. JR, BINKERT, F, BOUE, J, CORBIN, E, CROQUETTE, M. F, GILGENKRANTZ, S, DE GROUCHY, J, BERTHEAS, M. F, PRIEUR, M, RAOUL, O, SERVILLE, F, LEWIS, J. G, SIFFROI, J. P, THEPOT, F, LEJEUNE, J, ANTONARAKIS, S. E, ADELSBERGER, F. A, PETERSEN, M. B, SERRE, J.-L, RETHORE, M.-O, DE BLOIS, M.-C, PARENT, P, SCHINZEL, A. A

Volltext

Excessive glutamine sensitivity in Alzheimer's disease and Down syndrome lymphocytes von Peeters, Marie A., Salabelle, Aline, Attal, Nadine, Rethore, Marie-Odile, Mircher, Clothilde, Laplane, Dominique, Lejeune, Jérôme

Volltext

No association between common polymorphisms in genes of folate and homocysteine metabolism and the risk of Down's syndrome among French mothers von Chango, Abalo, Fillon-Emery, Nathalie, Mircher, Clotilde, Bléhaut, Henri, Lambert, Daniel, Herbeth, Bernard, James, S. Jill, Réthoré, Marie-Odile, Nicolas, Jean Pierre

Volltext

Cystathionine beta synthase: Gene dosage effect in trisomy 21 von Chadefaux, B., Rethoré, M.O., Raoul, O., Ceballos, I., Poissonnier, M., Gilgenkranz, S., Allard, D.

Volltext

Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region von Chettouh, Z, Croquette, M F, Delobel, B, Gilgenkrants, S, Leonard, C, Maunoury, C, Prieur, M, Rethoré, M O, Sinet, P M, Chery, M

Volltext

Métabolisme des substrats monocarbonés et trisomie 21: analyse de l'impact des polymorphismes génétiques von CHANGE, A, MIRCHER, C, JAMES, S. J, RETHORE, M. O, NICOLAS, J.-P

Volltext

Homocysteine concentrations in adults with trisomy 21: effect of B vitamins and genetic polymorphisms von Fillon-Emery, N, Chango, A, Mircher, C, Barbe, F, Blehaut, H, Herbeth, B, Rosenblatt, D.S, Rethore, M.O, Lambert, D, Nicolas, J.P

Volltext

Parents âgés et handicapés vieillissants : une situation nouvelle, un essai de réponse : Vieillissement des handicapés mentaux von PELLERIN, D, RETHORE, M.-O, PELLERIN, P

Volltext

Homocysteine and the methotrexate toxicity in trisomy 21 von LEJEUNE, J, PEETERS, M, RETHORE, M.-O, DE BLOIS, M.-C

Volltext

La mélatonine, pour quoi faire ? Discussion von TOUITOU, Yvan, SWYNGHEDAUW, M. Bernard, PHILIPPON, M. Jacques, MOLINA, M. Claude, RETHORE, M, LOO, M. Henri, BATTIN, M. Jacques, HAMON, M. Michel

Volltext

Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases von Lespinasse, J., Réthoré, M.O., North, M.O., Bovier-Lapierre, M., Lundsteen, C., Fert-Ferrer, S., Bugge, M., Kirchoff, M.

Volltext