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M F Croquette

Showing results (21-30 of 48) with videos related to

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LARC Medical|March 1, 1983
[Constitution 48, XXYY or the double-male syndrome]G Vittu, M F Croquette, H Ducoulombier, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|January 1, 1991
[Cytogenetic anomalies after isotope synoviorthesis in rheumatoid polyarthritis]E Houvenagel, L Debouvry, O Leloire, et al.
Journal of Medical Genetics|December 1, 1998
Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication studyC Stavropoulou, C Mignon, B Delobel, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effectC Mignon, P Malzac, A Moncla, et al.
Human Genetics|July 18, 1979
Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21)J Couturier, B Dutrillaux, P Garber, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X;Y translocationO Gabriel-Robez, Y Rumpler, C Ratomponirina, et al.
Journal of Medical Genetics|April 1, 1993
Characterisation of a highly polymorphic microsatellite at the DXS207 locus: confirmation of very close linkage to the retinoschisis disease geneC Oudet, C Weber, J Kaplan, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Human somatic chromosome chains and rings. A preliminary note on end-to-end fusionB Dutrillaux, M F Croquette, E Viegas-Pequignot, et al.
American Journal of Medical Genetics|April 1, 1992
Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic associationI Oberlé, J Boué, M F Croquette, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Unusual mechanism in Prader-Willi syndrome: incidence in genetic counseling]S Klosowski, B Delobel, C Morisot, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
LARC Medical|March 1, 1983
[Constitution 48, XXYY or the double-male syndrome]G Vittu, M F Croquette, H Ducoulombier, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|January 1, 1991
[Cytogenetic anomalies after isotope synoviorthesis in rheumatoid polyarthritis]E Houvenagel, L Debouvry, O Leloire, et al.
Journal of Medical Genetics|December 1, 1998
Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication studyC Stavropoulou, C Mignon, B Delobel, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Clinical heterogeneity in 16 patients with inv dup 15 chromosome: cytogenetic and molecular studies, search for an imprinting effectC Mignon, P Malzac, A Moncla, et al.
Human Genetics|July 18, 1979
Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21)J Couturier, B Dutrillaux, P Garber, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X;Y translocationO Gabriel-Robez, Y Rumpler, C Ratomponirina, et al.
Journal of Medical Genetics|April 1, 1993
Characterisation of a highly polymorphic microsatellite at the DXS207 locus: confirmation of very close linkage to the retinoschisis disease geneC Oudet, C Weber, J Kaplan, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Human somatic chromosome chains and rings. A preliminary note on end-to-end fusionB Dutrillaux, M F Croquette, E Viegas-Pequignot, et al.
American Journal of Medical Genetics|April 1, 1992
Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic associationI Oberlé, J Boué, M F Croquette, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Unusual mechanism in Prader-Willi syndrome: incidence in genetic counseling]S Klosowski, B Delobel, C Morisot, et al.
Pageof 5