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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.
Arthritis and Rheumatism|August 16, 2000
Randomized, placebo-controlled, crossover trial of low-dose oral methotrexate in children with extended oligoarticular or systemic arthritisP Woo, T R Southwood, A M Prieur, et al.
American Journal of Human Genetics|July 1, 1995
Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 regionZ Chettouh, M F Croquette, B Delobel, et al.
American Journal of Human Genetics|December 1, 1992
No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21C Pangalos, D Théophile, P M Sinet, et al.
Clinical and Experimental Rheumatology|May 1, 1990
Is onset type evaluated during the first 3 months of disease satisfactory for defining the sub-groups of juvenile chronic arthritis? A EULAR Cooperative Study (1983-1986)A M Prieur, B M Ansell, R Bardfeld, et al.
American Journal of Human Genetics|March 1, 1994
Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysisC Pangalos, D Avramopoulos, J L Blouin, et al.
Annales De Genetique|January 1, 1997
Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour pronenessM Bahuau, D Vidaud, M Kujas, et al.
Annales De Genetique|January 1, 1992
Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new casesM Poissonnier, C Turleau, M Olivier-Martin, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1989
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndromeZ Rahmani, J L Blouin, N Creau-Goldberg, et al.
American Journal of Medical Genetics|December 18, 1996
Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis associationM Bahuau, W Flintoff, B Assouline, et al.
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