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Neuropediatrics|August 12, 2003
Familial bilateral medial parietooccipital band heterotopia not related to DCX or LIS1 gene defectsN Deconinck, T Duprez, V des Portes, et al.
American Journal of Hematology|September 1, 1988
Atypical haplotypes linked to the beta S gene in Africa are likely to be the product of recombinationR Srinivas, O Dunda, R Krishnamoorthy, et al.
Annales De Cardiologie Et D'Angeiologie|March 1, 1996
[Imaging in cardiac hydatid cyst. Apropos of a case]A Bennis, S Chraïbi, M Noureddine, et al.
American Journal of Hematology|August 1, 1992
Presence of an African beta-globin gene cluster haplotype in normal chromosomes in SicilyA Ragusa, V Frontini, M Lombardo, et al.
Human Biology|June 1, 1991
Origin and spread of beta-globin gene mutations in India, Africa, and Mediterranea: analysis of the 5' flanking and intragenic sequences of beta S and beta C genesG Trabuchet, J Elion, G Baudot, et al.
American Journal of Medical Genetics|July 9, 1999
Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54)L B Jemaa, V des Portes, R Zemni, et al.
Biotechniques|March 5, 2003
DHPLC-based method for DNA methylation analysis of differential methylated regions from imprinted genesP Couvert, K Poirier, A Carrié, et al.
Human Heredity|January 1, 1982
Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia traitC Junien, A Chaventré, Y Fofana, et al.
Annales De Genetique|January 1, 1987
[Autosomal recessive spondylometaphyseal dysplasia. Apropos of 3 familial cases]A O Meziane, A Meziane, M Ksiyer, et al.
Acta Haematologica|January 1, 1976
Congenital enzymopenic methaemoglobinaemia. Clinical and biochemical study of a family with three homozygotesA Mast, R Milo, C Junien, et al.
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