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N Morichon

Showing results (1-10 of 31) with videos related to

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Prenatal Diagnosis|December 1, 1990
Duplication of the long arm of chromosome 13 secondary to a recombination in a maternal intrachromosomal insertion (shift)M Vekemans, N Morichon-Delvallez
Revue Francaise De Gynecologie Et D'Obstetrique|April 1, 1985
[Paracentric inversion: a study of 2 new cases]N Morichon-Delvallez, F Marchand
Annales De Genetique|January 1, 1985
[Paracentric inversions in man. Apropos of 2 familial observations]N Morichon-Delvallez, F Marchand
Human Genetics|January 1, 1985
Deletion of band 13q21 is compatible with normal phenotypeJ Couturier, N Morichon-Delvallez, B Dutrillaux
Annales De Genetique|January 1, 1982
[Attenuated phenotype of trisomy 4p by translocation t(X;4)(p21.2;p13)]N Morichon-Delvallez, J Couturier, B Frison
Annales De Genetique|January 1, 1988
Inherited Xq duplication due to a zygotic translocation t(X;X)(q23;q27)N Morichon-Delvallez, J Couturier, V Bourdrel
European Journal of Human Genetics : EJHG|January 1, 1997
Prenatal diagnosis in FranceS Aymé, N Morichon, J Goujard, et al.
Journal of Medical Genetics|June 1, 1993
Holoprosencephaly and sacral agenesis in a fetus with a terminal deletion 7q36-->7qterN Morichon-Delvallez, A L Delezoide, M Vekemans
Prenatal Diagnosis|April 1, 1993
Trisomy 15 in chorionic villi and Prader-Willi syndrome at birthN Morichon-Delvallez, P Mussat, Y Dumez, et al.
Archives Francaises De Pediatrie|May 1, 1983
[Hypopituitarism, median dysraphia, and chromosomal aberrations]B Boudailliez, N Morichon-Delvallez, B Cuvelier, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Prenatal Diagnosis|December 1, 1990
Duplication of the long arm of chromosome 13 secondary to a recombination in a maternal intrachromosomal insertion (shift)M Vekemans, N Morichon-Delvallez
Revue Francaise De Gynecologie Et D'Obstetrique|April 1, 1985
[Paracentric inversion: a study of 2 new cases]N Morichon-Delvallez, F Marchand
Annales De Genetique|January 1, 1985
[Paracentric inversions in man. Apropos of 2 familial observations]N Morichon-Delvallez, F Marchand
Human Genetics|January 1, 1985
Deletion of band 13q21 is compatible with normal phenotypeJ Couturier, N Morichon-Delvallez, B Dutrillaux
Annales De Genetique|January 1, 1982
[Attenuated phenotype of trisomy 4p by translocation t(X;4)(p21.2;p13)]N Morichon-Delvallez, J Couturier, B Frison
Annales De Genetique|January 1, 1988
Inherited Xq duplication due to a zygotic translocation t(X;X)(q23;q27)N Morichon-Delvallez, J Couturier, V Bourdrel
European Journal of Human Genetics : EJHG|January 1, 1997
Prenatal diagnosis in FranceS Aymé, N Morichon, J Goujard, et al.
Journal of Medical Genetics|June 1, 1993
Holoprosencephaly and sacral agenesis in a fetus with a terminal deletion 7q36-->7qterN Morichon-Delvallez, A L Delezoide, M Vekemans
Prenatal Diagnosis|April 1, 1993
Trisomy 15 in chorionic villi and Prader-Willi syndrome at birthN Morichon-Delvallez, P Mussat, Y Dumez, et al.
Archives Francaises De Pediatrie|May 1, 1983
[Hypopituitarism, median dysraphia, and chromosomal aberrations]B Boudailliez, N Morichon-Delvallez, B Cuvelier, et al.
Pageof 4