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The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Molecular basis of haemoglobinopathies and G6PD deficiency in the Comorian populationC Badens, F Martinez di Montemuros, I Thuret, et al.
Clinical Rheumatology|August 15, 2000
A first molecular approach towards CGG repeat expansion in FMR1 gene in systemic lupus erythematosus and in Sjögren's syndrome: a preliminary reportB Granel, V Ravix, K Pedeillier, et al.
Journal of Medical Genetics|July 29, 1999
Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counsellingA Moncla, P Malzac, M O Livet, et al.
American Journal of Human Genetics|June 1, 1993
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21)P Saugier-Veber, V Abadie, A Moncla, et al.
Human Genetics|April 1, 1989
Localization of human platelet proteoglycan gene to chromosome 10, band q22.1, by in situ hybridizationM G Mattei, J P Périn, P M Alliel, et al.
Presse Medicale (Paris, France : 1983)|February 3, 1996
[Genetic hemoglobin diseases. Prevention at centers for family planning and education of maternal-child protection in Marseille]D Lena-Russo, N Erny, F Serradimigni, et al.
Human Genetics|March 1, 1989
Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardationM A Voelckel, N Philip, C Piquet, et al.
Genomics|November 1, 1989
CpG dinucleotides are mutation hot spots in phenylketonuriaV Abadie, S Lyonnet, N Maurin, et al.
American Journal of Human Genetics|March 1, 1990
Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21J L Blouin, Z Rahmani, Z Chettouh, et al.
Medecine Tropicale : Revue Du Corps De Sante Colonial|January 13, 2012
[Study of treatment adherence by patients living with HIV in 2009 at the outpatient care and treatment center of Brazzaville, Congo]N Faure, M Diafouka, P Nzounza, et al.
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