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M C Pellissier

Showing results (1-10 of 11) with videos related to

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Pediatrie|January 1, 1992
[Fragile X syndrome: current knowledge]M C Pellissier, M A Voelckel, J F Mattei
Prenatal Diagnosis|March 17, 2000
Fetoplacental chromosomal discrepancyC Farra, B Giudicelli, M C Pellissier, et al.
Journal De Genetique Humaine|January 1, 1988
[Balanced chromosome rearrangements with abnormal phenotype]N Philip, M G Mattei, M C Pellissier, et al.
American Journal of Medical Genetics|February 1, 1991
Transmission of mental retardation with fragile X site by two normal transmitter brothersM C Pellissier, M A Voelckel, C Piquet, et al.
Human Genetics|January 1, 1987
Monosomy 21: a new case confirmed by in situ hybridizationM C Pellissier, N Philip, M A Voelckel-Baeteman, et al.
Human Genetics|November 1, 1988
Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridizationM C Pellissier, M Laffage, N Philip, et al.
Prenatal Diagnosis|April 1, 1992
Prenatal diagnosis of Fryns' syndromeM C Pellissier, N Philip, A Potier, et al.
American Journal of Medical Genetics|February 1, 1991
Fragile X syndrome in an extended family with special reference to an affected male with Klinefelter syndromeM A Voelckel, M C Pellissier, C Piquet, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Unexpected inheritance of the (CGG)n trinucleotide expansion in a fragile X syndrome familyP Malzac, V Biancalana, M A Voelckel, et al.
Human Genetics|March 1, 1989
Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardationM A Voelckel, N Philip, C Piquet, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Pediatrie|January 1, 1992
[Fragile X syndrome: current knowledge]M C Pellissier, M A Voelckel, J F Mattei
Prenatal Diagnosis|March 17, 2000
Fetoplacental chromosomal discrepancyC Farra, B Giudicelli, M C Pellissier, et al.
Journal De Genetique Humaine|January 1, 1988
[Balanced chromosome rearrangements with abnormal phenotype]N Philip, M G Mattei, M C Pellissier, et al.
American Journal of Medical Genetics|February 1, 1991
Transmission of mental retardation with fragile X site by two normal transmitter brothersM C Pellissier, M A Voelckel, C Piquet, et al.
Human Genetics|January 1, 1987
Monosomy 21: a new case confirmed by in situ hybridizationM C Pellissier, N Philip, M A Voelckel-Baeteman, et al.
Human Genetics|November 1, 1988
Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridizationM C Pellissier, M Laffage, N Philip, et al.
Prenatal Diagnosis|April 1, 1992
Prenatal diagnosis of Fryns' syndromeM C Pellissier, N Philip, A Potier, et al.
American Journal of Medical Genetics|February 1, 1991
Fragile X syndrome in an extended family with special reference to an affected male with Klinefelter syndromeM A Voelckel, M C Pellissier, C Piquet, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Unexpected inheritance of the (CGG)n trinucleotide expansion in a fragile X syndrome familyP Malzac, V Biancalana, M A Voelckel, et al.
Human Genetics|March 1, 1989
Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardationM A Voelckel, N Philip, C Piquet, et al.
Pageof 2