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Annales De Genetique|January 1, 1992
Incontinentia pigmenti (type 1) and X;5 translocationP Bitoun, C Philippe, M Cherif, et al.
Annales De Genetique|January 1, 1991
Segregation analysis of autosomal fragile sites in three families with the fragile X chromosomeC Barletta, R M Ragusa, G Garofalo, et al.
Annales De Genetique|January 1, 1991
Slide Flask direct amniotic fluid culturesJ Montagut, E Carles
Annales De Genetique|January 1, 1990
Tandem duplication of proximal 5qA Rojas-Martinez, D Garcia-Cruz, C Medina, et al.
Annales De Genetique|January 1, 1990
Partial trisomy 17q and monosomy 9p due to a familial translocationP D Cotter, N L Stewart
Annales De Genetique|January 1, 1990
CYP21B gene conversion and complete CYP21A gene deletion in congenital adrenal hyperplasiaJ M Lobaccaro, N Ghanem, G Lefranc, et al.
Annales De Genetique|January 1, 1991
Branchial arch anomalies in trisomy 18A Verloes, N Seret, V Bernier, et al.
Annales De Genetique|January 1, 1991
69,XXX karyotype in a malformed liveborn female. Maternal origin of triploidyF Galán, F Orts, M S Aguilar, et al.
Annales De Genetique|January 1, 1991
Full trisomy 22 in a malformed newborn femaleM A Feret, F Galán, M S Aguilar, et al.
Annales De Genetique|January 1, 1985
[Genetic polymorphism of drepanocytosis]J Pagnier, H Wajcman, V Baudin, et al.
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