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Annales De Genetique|January 1, 1995
Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndromeK Devriendt, K De Mars, P De Cock, et al.Annales De Genetique|January 1, 1996
[Causal mutation or rare polymorphism? Frequency of mutation not found in 3 chromosome is less than 3 divided by n]M JeanpierreAnnales De Genetique|January 1, 1987
Partial monosomy 15q due to de novo t(15;22)(q15;p11)M A Mori, L Rodriguez, I Pinel, et al.Annales De Genetique|January 1, 1987
Rare syndromes. The Kaufman-McKusick syndrome. A review of the 44 cases reported in the literatureA Cantani, M L Tacconi, N Benincori, et al.Annales De Genetique|January 1, 1979
Familial paracentric inversion of the short arm of chromosome 3J P Fryns, H van den BergheAnnales De Genetique|January 1, 1987
Moderate mental retardation and mild dysmorphic syndrome in proximal 7q interstitial deletionJ P Fryns, A Kleczkowska, H Van den BergheAnnales De Genetique|January 1, 1987
Recurrent HSR in the centromeric region of chromosome 8 in breast cancerM Gerbault-Seureau, P Vielh, B DutrillauxAnnales De Genetique|January 1, 1986
Paracentric inversions in man. A French collaborative study. Groupe de Cytogénéticiens FrançaisAnnales De Genetique|January 1, 1987
[Autosomal recessive spondylometaphyseal dysplasia. Apropos of 3 familial cases]A O Meziane, A Meziane, M Ksiyer, et al.Pageof 129