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M F Croquette

Showing results (41-50 of 48) with videos related to

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Journal of Medical Genetics|February 12, 2002
Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardationA M Lossi, F Laugier-Anfossi, D Depetris, et al.
International Journal of Cancer|June 19, 2001
Cancer risk in heterozygotes for ataxia-telangiectasiaB Geoffroy-Perez, N Janin, K Ossian, et al.
Psychiatry Research|October 1, 1998
Genotype-phenotype relationship in female carriers of the premutation and full mutation of FMR-1P Franke, M Leboyer, M Gänsicke, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 1, 1997
[Fragile X syndrome is still unrecognized: efficacy of molecular diagnosis in mentally retarded probands]M Cossée, C Moutou, V Biancalana, et al.
Journal of Medical Genetics|September 10, 2003
Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observationsJ J Luciani, P de Mas, D Depetris, et al.
Journal of Medical Genetics|April 6, 2001
Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardationF Giraudeau, L Taine, V Biancalana, et al.
Annales De Genetique|January 1, 1997
Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children)M Mathieu, C Piussan, F Thepot, et al.
Annales De Genetique|July 18, 2002
French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literatureI Luquet, F Mugneret, P D Athis, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Journal of Medical Genetics|February 12, 2002
Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardationA M Lossi, F Laugier-Anfossi, D Depetris, et al.
International Journal of Cancer|June 19, 2001
Cancer risk in heterozygotes for ataxia-telangiectasiaB Geoffroy-Perez, N Janin, K Ossian, et al.
Psychiatry Research|October 1, 1998
Genotype-phenotype relationship in female carriers of the premutation and full mutation of FMR-1P Franke, M Leboyer, M Gänsicke, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 1, 1997
[Fragile X syndrome is still unrecognized: efficacy of molecular diagnosis in mentally retarded probands]M Cossée, C Moutou, V Biancalana, et al.
Journal of Medical Genetics|September 10, 2003
Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observationsJ J Luciani, P de Mas, D Depetris, et al.
Journal of Medical Genetics|April 6, 2001
Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardationF Giraudeau, L Taine, V Biancalana, et al.
Annales De Genetique|January 1, 1997
Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children)M Mathieu, C Piussan, F Thepot, et al.
Annales De Genetique|July 18, 2002
French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literatureI Luquet, F Mugneret, P D Athis, et al.
Pageof 5