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British Journal of Haematology|March 1, 1997
The relative importance of the X-linked FCP locus and beta-globin haplotypes in determining haemoglobin F levels: a study of SS patients homozygous for beta S haplotypesY P Chang, M Maier-Redelsperger, K D Smith, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infectionsM G Neonato, C Y Lu, M Guilloud-Bataille, et al.
American Journal of Human Genetics|June 13, 1998
Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation databaseC Jeanpierre, E Denamur, I Henry, et al.
American Journal of Hematology|January 12, 2000
Atypical beta(s) haplotypes are generated by diverse genetic mechanismsM A Zago, W A Silva, B Dalle, et al.
Human Mutation|November 26, 1999
Compound SFTPB 1549C-->GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiencyM Tredano, R M van Elburg, A G Kaspers, et al.
Annales De Genetique|January 1, 1997
Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded childrenB Gérard, M F Le Heuzey, G Brunie, et al.
European Journal of Haematology|September 28, 2000
Acute clinical events in 299 homozygous sickle cell patients living in France. French Study Group on Sickle Cell DiseaseM G Neonato, M Guilloud-Bataille, P Beauvais, et al.
American Journal of Physical Anthropology|July 28, 1999
Genetic diversity of two African and sixteen South American populations determined on the basis of six hypervariable lociW A Da Silva, M C Bortolini, D Meyer, et al.
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