Annales de Genetique

A constitutional translocation t(1;4)(p21;p15) in a case of chronic lymphocytic leukemia
pp. 169-171(3)
Authors: Eclache V.; Benzacken B.; Kettaneh A.; Fain O.

Distal trisomy 14 (q24 -> qter) and aorto-pulmonary window: a case report and review of the literature
pp. 173-175(3)
Authors: Perrin Y.; Addor M.-C.; Sekarski N.; Gaide A.-C.; Schorderet D.F.

Tetraploid/diploid mosaicism: case report and review of the literature
pp. 177-180(4)
Authors: Alonso L.; Melaragno I.; Bortolai A.; Takeno S.; Brunoni D.

A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype
pp. 181-183(3)
Authors: Ozkul Y.; Emre Atabek M.; Dundar M.; Kurtoglu S.; Saatci C.

A family with two different chromosomal translocations
pp. 185-187(3)
Authors: Ozkul Y.; Dundar M.

Use of two FISH probes provides a cost-effective, simple protocol to exclude an imprinting centre defect in routine laboratory testing for suspected Prader-Willi and Angelman syndrome
pp. 189-191(3)
Authors: Smith A.; Robson L.; Heaps L.S.

Chromosome studies of in vitro senescent lymphocytes: nonrandom trisomy 2
pp. 193-196(4)
Authors: Busson-Le Coniat M.; Boucher N.; Blanche H.; Thomas G.; Berger R.

GM polymorphism and the evolutionary history of modern humans
pp. 197-206(10)
Author: Chaabani H.

Auricular mild errors of morphogenesis: epidemiological study with application of a targeted computer program
pp. 207-212(6)
Authors: Grun M.; Merlob P.; Grunfeld A.; Abend M.; Chystiakov I.; Riskin-Mashiah S.; Bader D.

Haploinsufficiency of TBX3 causes ulnar-mammary syndrome in a large Turkish family
pp. 213-217(5)
Authors: Wollnik B.; Kayserili H.; Uyguner O.; Tukel T.; Yuksel-Apak M.

Screening for mutations in the gene for phosphorylation kinase 1 in Silver-Russell syndrome patients
pp. 219-221(3)
Authors: Mavany M.; Wollmann H.A.; Eggermann T.