Annales de Genetique

Trisomy 4q syndrome: presentation of a new case and review of the literature
pp. 53-57(5)
Authors: Lundin C.; Zech L.; Sjors K.; Wadelius C.; Anneren G.

Long-term follow-up of a girl with oro-facio-digital syndrome type I due to a mutation in the OFD 1 gene
pp. 59-62(4)
Authors: Stoll C.; Sauvage P.

True vs. false inv(Y)(p11q11.2): a familial instance concurrent with trisomy 21
pp. 63-65(3)
Authors: Rivera H.; Gutierrez-Angulo M.; Gomez-Sanchez H.; Macias-Gomez N.; Barros-Nunez P.

A novel translocation, t(9;21)(q13;q22) rearranging the RUNX1 gene in acute myelomonocytic leukemia
pp. 67-69(3)
Authors: Paulien S.; Maarek O.; Daniel M.-T.; Berger R.

Genetic instability in human mismatch repair deficient cancers
pp. 71-75(5)
Authors: Duval A.; Hamelin R.

French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literature
pp. 77-88(12)
Authors: Luquet I.; Mugneret F.; Athis P.D.; Nadal N.; Favre B.; Abel C.; Chelloug N.; Lespinasse J.; Portnoi M.F.; Joye N.; Dupont J.M.; Lebbar A.; Bresson J.L.; Fellmann F.; Siffroi J.P.; Chantot-Bastaraud S.; Chiesa J.; Amblard F.; Devillard F.; Jeandidier E.; Boceno M.; Rival J.M.; Bellec V.; Lallaoui H.; Delobel B.; Croquette M.F.; Benzacken B.

The psychopathological phenotype of velo-cardio-facial syndrome
pp. 89-95(7)
Authors: Vogels A.; Verhoeven W.M.A.; Tuinier S.; DeVriendt K.; Swillen A.; Curfs L.M.G.; Frijns J.P.

The Peters' plus syndrome: a review
pp. 97-103(7)
Authors: Maillette de Buy Wenniger-Prick L.J.J.M.; Hennekam R.C.M.