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H Ledbetter

Showing results (301-310 of 388) with videos related to

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American Journal of Human Genetics|March 7, 2001
Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangementsS Giglio, K W Broman, N Matsumoto, et al.
Genomics|August 1, 1989
Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17A G Menon, D H Ledbetter, D C Rich, et al.
American Journal of Human Genetics|January 1, 1989
Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17J W Fountain, M R Wallace, A M Brereton, et al.
Science (New York, N.Y.)|July 26, 1996
Multicolor spectral karyotyping of human chromosomesE Schröck, S du Manoir, T Veldman, et al.
Biological Psychiatry|October 18, 2024
Advancing Mental Health Research Through Strategic Integration of Transdiagnostic Dimensions and GenomicsAlysa E Doyle, Carrie E Bearden, Raquel E Gur, et al.
Genomics|September 11, 1991
Assignment of the human prohibitin gene (PHB) to chromosome 17 and identification of a DNA polymorphismJ J White, D H Ledbetter, R L Eddy, et al.
Prenatal Diagnosis|May 1, 1992
Chorionic mosaicism: association with fetal loss but not with adverse perinatal outcomeR J Wapner, J L Simpson, M S Golbus, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Medical manifestations and health care utilization among adult MyCode participants with neurodevelopmental psychiatric copy number variantsBrenda Finucane, Matthew T Oetjens, Alicia Johns, et al.
Prenatal Diagnosis|December 11, 1999
Satellited chromosome 10 detected prenatally in a fetus and confirmed as mosaic in a parentP D Storto, T N Diehn, D P O'Malley, et al.
Human Molecular Genetics|November 18, 1998
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformationD T Pilz, N Matsumoto, S Minnerath, et al.
Pageof 39

Showing results (301-310 of 388) with videos related to

Sort By:
Pageof 39
American Journal of Human Genetics|March 7, 2001
Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangementsS Giglio, K W Broman, N Matsumoto, et al.
Genomics|August 1, 1989
Characterization of a translocation within the von Recklinghausen neurofibromatosis region of chromosome 17A G Menon, D H Ledbetter, D C Rich, et al.
American Journal of Human Genetics|January 1, 1989
Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17J W Fountain, M R Wallace, A M Brereton, et al.
Science (New York, N.Y.)|July 26, 1996
Multicolor spectral karyotyping of human chromosomesE Schröck, S du Manoir, T Veldman, et al.
Biological Psychiatry|October 18, 2024
Advancing Mental Health Research Through Strategic Integration of Transdiagnostic Dimensions and GenomicsAlysa E Doyle, Carrie E Bearden, Raquel E Gur, et al.
Genomics|September 11, 1991
Assignment of the human prohibitin gene (PHB) to chromosome 17 and identification of a DNA polymorphismJ J White, D H Ledbetter, R L Eddy, et al.
Prenatal Diagnosis|May 1, 1992
Chorionic mosaicism: association with fetal loss but not with adverse perinatal outcomeR J Wapner, J L Simpson, M S Golbus, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Medical manifestations and health care utilization among adult MyCode participants with neurodevelopmental psychiatric copy number variantsBrenda Finucane, Matthew T Oetjens, Alicia Johns, et al.
Prenatal Diagnosis|December 11, 1999
Satellited chromosome 10 detected prenatally in a fetus and confirmed as mosaic in a parentP D Storto, T N Diehn, D P O'Malley, et al.
Human Molecular Genetics|November 18, 1998
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformationD T Pilz, N Matsumoto, S Minnerath, et al.
Pageof 39