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M A Voelckel

Showing results (1-10 of 25) 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
American Journal of Medical Genetics|February 24, 2001
Fragile X syndrome and 22q11.2 microdeletion in the same sibshipC Missirian, A Moncla, M A Voelckel, et al.
FEBS Letters|April 19, 1993
Characterization of cAMP dependent CFTR-chloride channels in human tracheal gland cellsF Becq, M D Merten, M A Voelckel, 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.
American Journal of Medical Genetics|July 24, 1998
Atypical molecular findings identify limits of technical screening tests for Prader-Willi and Angelman syndrome diagnosesP Malzac, A Moncla, K Pedeillier, et al.
Journal of Genetic Counseling|May 22, 2013
French professionals in genetic counselor careersC Cordier, N Taris, A De Pauw, 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|December 1, 1988
Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardationM A Voelckel, M G Mattei, C N'Guyen, et al.
Journal De Genetique Humaine|June 1, 1989
[Linkage studies in Emery-Dreifuss muscular dystrophy]V Paquis, N Philip, M A Voelckel, 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.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Pediatrie|January 1, 1992
[Fragile X syndrome: current knowledge]M C Pellissier, M A Voelckel, J F Mattei
American Journal of Medical Genetics|February 24, 2001
Fragile X syndrome and 22q11.2 microdeletion in the same sibshipC Missirian, A Moncla, M A Voelckel, et al.
FEBS Letters|April 19, 1993
Characterization of cAMP dependent CFTR-chloride channels in human tracheal gland cellsF Becq, M D Merten, M A Voelckel, 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.
American Journal of Medical Genetics|July 24, 1998
Atypical molecular findings identify limits of technical screening tests for Prader-Willi and Angelman syndrome diagnosesP Malzac, A Moncla, K Pedeillier, et al.
Journal of Genetic Counseling|May 22, 2013
French professionals in genetic counselor careersC Cordier, N Taris, A De Pauw, 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|December 1, 1988
Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardationM A Voelckel, M G Mattei, C N'Guyen, et al.
Journal De Genetique Humaine|June 1, 1989
[Linkage studies in Emery-Dreifuss muscular dystrophy]V Paquis, N Philip, M A Voelckel, 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.
Pageof 3