Annales de Genetique

Author index
pp. I-I(1)

Keyword index
pp. III-IV(2)

The history of cytogenetics Portraits of some pioneers
pp. 433-442(10)
Authors: Gilgenkrantz S.; Rivera E.M.

FISH and PCR analyses in three patients with 45,X/46,X,idic(Y) karyotype: clinical and pathologic spectrum
pp. 443-448(6)
Authors: Alvarez-Nava F.; Soto M.; Martinez M.C.; Prieto M.; Alvarez Z.

Duane anomaly, congenital myopathy and severe scoliosis in sibs: new AR syndrome?
pp. 449-452(4)
Authors: Verloes A.; Misson J.-P.; Gillet P.; Baumann C.; Spiritus M.; Deprez M.

Familial interstitial deletion of chromosome 4 (p15.2p16.1)
pp. 453-458(6)
Authors: Tonk V.S.; Jalal S.M.; Gonzalez J.; Kennedy A.; Velagaleti G.V.N.

Limb reduction defects in the first generation and deafness in the second generation of intrauterine exposed fetuses to diethylstilbestrol
pp. 459-465(7)
Authors: Stoll C.; Alembik Y.; Dott B.

Gerstmann-Straussler-Scheinker disease with P102L-V129 mutation: a case with psychiatric manifestations at onset
pp. 467-469(3)
Authors: Bianca M.; Bianca S.; Vecchio I.; Raffaele R.; Ingegnosi C.; Nicoletti F.

De novo balanced translocation (2;10)(q24;q22) associated with mental retardation
pp. 471-473(3)
Authors: Santos C.B.; Discepoli G.; Pigliapoco F.; Boy R.; Pimentel M.M.G.

Paternal reciprocal translocation t(11;16)(p13;q24.3) in a Silver-Russel syndrome patient
pp. 475-478(4)
Authors: Rao V.B.; Lily K.; Seema K.; Ghosh K.; Dipika M.

Two 48,XXYY patients: clinical, cytogenetic and molecular aspects
pp. 479-481(3)
Authors: Zelante L.; Piemontese M.R.; Francioli G.; Calvano S.

''Cri-du-chat'' syndrome in a patient born to a mother with a paracentric inversion of chromosome 5q
pp. 483-486(4)
Authors: Bourthoumieu S.; Esclaire F.; Terro F.; Baclet M.C.; Bedu A.; Dufetelle B.; Gilbert B.; Barthe D.; Yardin C.