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Annales De Genetique|January 1, 1991
Routine autoradiographic analysis of DNA excision-repair. Report of prenatal and postnatal diagnosis in eleven familiesJ B Savary, F Vasseur, M M DeminattiAnnales De Genetique|January 1, 1991
Lethal progeroid syndrome with osteolysis. Case reportM Le Merrer, M Guillot, M L Briard, et al.Annales De Genetique|January 1, 1991
Pericentric inversion of the X chromosome: presentation of a case and review of the literatureD F Schorderet, C Friedman, C M DistecheAnnales De Genetique|January 1, 1979
[Sex linked mental deficiency, unusual facies, macroorchidism and fragile site on chromosome X (author's transl)]C Turleau, P Czernichow, R Gorin, et al.Annales De Genetique|January 1, 1979
[De novo monosomy 4q32.1 leads to 4qter in a newborn with multiple malformations (author's transl)]M O Rethoré, J Couturier, J C Mselati, et al.Annales De Genetique|January 1, 1979
Malformed genitalia in the 47,XYY genotypeH Rivera, A Hernandez, R Martinez y Martinez, et al.Annales De Genetique|January 1, 1979
On the deletion 4p16 Wolf-Hirschhorn syndromeF Rivas, A Hernandez, Z Nazara, et al.Annales De Genetique|January 1, 1990
Small marker chromosomes in a series of 1,000 prenatal diagnoses by amniocentesisJ L Carrasco Juan, A Otero Gómez, M C Vilar Mesa, et al.Annales De Genetique|January 1, 1990
Clonal structural chromosomal rearrangements in lymphocytes of four patients with Werner's syndromeS Scappaticci, A Forabosco, G Borroni, et al.Annales De Genetique|January 1, 1989
A case of the ring 20 syndromeS G Thomsen, M B Petersen, E A Andersen, et al.Pageof 129