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Annales De Genetique|December 1, 1977
Deletion of the long arm of chromosome 4 [46,XX,del(4)(q31)] in a patient with congenital anomaliesE Back, C Hertel, W Vogel, et al.Annales De Genetique|January 1, 1979
[Ring chromosome 13 (author's transl)]A Hevia, M Bullon, A Novales, et al.Annales De Genetique|January 1, 1988
Complete trisomy 17p a relatively new syndromeJ T Martsolf, L Larson, S M Jalal, et al.Annales De Genetique|January 1, 1988
Hydrops fetalis as an indication for prenatal chromosome analysis with the example of the diagnosis of a duplication 15q11 and 17q25 due to a familial translocation 15/17G Schwanitz, K Zerres, M Niesen, et al.Annales De Genetique|January 1, 1988
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literatureG Palka, L Geraci, G Calabrese, et al.Annales De Genetique|January 1, 1986
46,XX,t(15;21)/47,XX,15p-,+21 mosaicism in a child with Down's syndromeJ Lucas, F Le Mee, K Pluquailec, et al.Annales De Genetique|January 5, 2002
18p deletion syndrome with a 45, XY, t (14; 18) (p11;q11.2), -18, karyotypeV B Rao, L Kerketta, S Korgaonkar, et al.Annales De Genetique|January 5, 2002
Duplication 8 [inv dup(8)(p12p23)] with macrocephalyV S Tonk, G N Wilson, G V VelagaletiAnnales De Genetique|February 13, 2001
Genetic differentiation of Yemeni people according to rhesus and Gm polymorphismsH Chaabani, A Sanchez-Mazas, S F SallamiPageof 129