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Annales De Genetique|September 1, 2004
Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18K Prabhakara, Herman E Wyandt, Xin L Huang, et al.
Annales De Genetique|January 1, 1992
Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndromeD M Ioan, C Maximilian, A Kleczkowska, et al.
Annales De Genetique|January 1, 1989
[Nucleolus organizer region--centromere translocation]M C de Blois, M O Rethoré, J Lejeune
Annales De Genetique|January 1, 1989
Partial trisomy 13q22----qter. A new caseF Galán, R García, M S Aguilar, et al.
Annales De Genetique|January 1, 1989
Severe midline fusion defects in a newborn with 10q26----qter deletionJ P Fryns, A Kleczkowska, H Fivez, et al.
Annales De Genetique|January 1, 1991
Association of the Hind III polymorphism with the androgen receptor gene in partial androgen insensitivity syndromeJ M Lobaccaro, C Belon, R Ruiz-Pacheco, et al.
Annales De Genetique|January 1, 1990
Usher syndrome type I is not linked to D1S81 (pTHH 33): evidence for genetic heterogeneityJ Kaplan, G Guasconi, D Bonneau, et al.
Annales De Genetique|January 1, 1991
Hypomelanosis of Ito: involvement of chromosome aberrations in this syndromeE Lenzini, P Bertoli, L Artifoni, et al.
Annales De Genetique|January 1, 1990
Study of the parental origin of sexual aneuploidy in ten families using RFLPsM Villamar, E Fernandez, C Ayuso, et al.
Annales De Genetique|January 1, 1990
Ring chromosome 16: a new caseM G Vianello, F Cottafava, D Bartoli, et al.
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