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Annales De Genetique|December 9, 2003
De novo balanced translocation (2;10)(q24;q22) associated with mental retardationCíntia Barros Santos, Giancarlo Discepoli, Francesco Pigliapoco, et al.
Annales De Genetique|December 9, 2003
Paternal reciprocal translocation t(11;16)(p13;q24.3) in a Silver-Russel syndrome patientVundinti Babu Rao, Kerketta Lily, Korgaonkar Seema, et al.
Annales De Genetique|December 9, 2003
"Cri-du-chat" syndrome in a patient born to a mother with a paracentric inversion of chromosome 5qSylvie Bourthoumieu, Françoise Esclaire, Faraj Terro, et al.
Annales De Genetique|June 9, 2004
A novel promoter polymorphism (-71C>T) in KRTHB6 gene in Indian populationNarendra K Bairwa, Dheeraj Malhotra, Anjana Saha, et al.
Annales De Genetique|June 9, 2004
Genealogical study of myotonic dystrophy in Istria (Croatia)I Medica, N Logar, D Leonardelli Mileta, et al.
Annales De Genetique|June 9, 2004
Apolipoprotein E gene polymorphism effects triglycerides but not CAD risk in Caucasian women younger than 65 yearsMitja Letonja, Barbara Guzic-Salobir, Borut Peterlin, et al.
Annales De Genetique|June 9, 2004
Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analysesM Velinov, H Gu, M Genovese, et al.
Annales De Genetique|January 1, 1992
Partial deletion 10p syndrome. Report of two patientsM G Obregon, R Mingarelli, A Giannotti, et al.
Annales De Genetique|January 1, 1992
Translocation t(22;22)(p11.1;q11.1) and NOR studies in a female with a history of repeated fetal lossA S Multani, U Radhakrishna, F J Sheth, et al.
Annales De Genetique|January 1, 1992
Trisomy 16 confined to chorionic villi and unfavourable outcome of pregnancyG Simoni, B Brambati, F Maggi, et al.
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