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Human Genetics|January 1, 1985
Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome)K E Davies, M G Mattei, J F Mattei, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patientsA Moncla, P Malzac, M A Voelckel, et al.
Sante (Montrouge, France)|February 4, 2009
[Ten years of commitment to persons living with HIV-AIDS: evaluation of the management in three ambulatory treatment centers of the French Red Cross in Africa]C Mouala, Y Madec, G Adam, 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.
Oncogene|January 1, 1990
Chromosomal localization of the three members of the jun proto-oncogene family in mouse and manM G Mattei, D Simon-Chazottes, S Hirai, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Down syndrome critical region around D21S55 on proximal 21q22.3Z Rahmani, J L Blouin, N Créau-Goldberg, et al.
Nature|June 2, 1986
The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy miceA Dautigny, M G Mattei, D Morello, et al.
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