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H Ledbetter

Showing results (271-280 of 388) with videos related to

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Human Genetics|July 1, 1991
Molecular characterization of a patient with del(1)(q23-q25)B Franco, L W Lai, D Patterson, et al.
Nature|January 3, 1991
Localization of the X inactivation centre on the human X chromosome in Xq13C J Brown, R G Lafreniere, V E Powers, et al.
American Journal of Human Genetics|January 1, 1989
Fine structure DNA mapping studies of the chromosomal region harboring the genetic defect in neurofibromatosis type IP O'Connell, R J Leach, D H Ledbetter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 31, 2022
Frequency of truncating FLCN variants and Birt-Hogg-Dubé-associated phenotypes in a health care system populationJuliann M Savatt, Hermela Shimelis, Andres Moreno-De-Luca, et al.
Human Genetics|May 1, 1987
Prenatal diagnosis of cystic fibrosis using linked DNA markers and microvillar intestinal enzyme analysisJ E Spence, G J Buffone, C L Rosenbloom, et al.
Journal of Neurogenetics|December 1, 1985
Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophyL H Yamaoka, R J Bartlett, D A Ross, et al.
Prenatal Diagnosis|May 1, 1992
Cytogenetic results from the U.S. Collaborative Study on CVSD H Ledbetter, J M Zachary, J L Simpson, et al.
American Journal of Human Genetics|February 1, 1988
Uniparental disomy as a mechanism for human genetic diseaseJ E Spence, R G Perciaccante, G M Greig, et al.
Genomics|May 23, 1998
The human ROX gene: genomic structure and mutation analysis in human breast tumorsC Lo Nigro, T Venesio, A Reymond, et al.
Clinical Genetics|June 14, 2000
Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15W P Robinson, S L Christian, B D Kuchinka, et al.
Pageof 39

Showing results (271-280 of 388) with videos related to

Sort By:
Pageof 39
Human Genetics|July 1, 1991
Molecular characterization of a patient with del(1)(q23-q25)B Franco, L W Lai, D Patterson, et al.
Nature|January 3, 1991
Localization of the X inactivation centre on the human X chromosome in Xq13C J Brown, R G Lafreniere, V E Powers, et al.
American Journal of Human Genetics|January 1, 1989
Fine structure DNA mapping studies of the chromosomal region harboring the genetic defect in neurofibromatosis type IP O'Connell, R J Leach, D H Ledbetter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 31, 2022
Frequency of truncating FLCN variants and Birt-Hogg-Dubé-associated phenotypes in a health care system populationJuliann M Savatt, Hermela Shimelis, Andres Moreno-De-Luca, et al.
Human Genetics|May 1, 1987
Prenatal diagnosis of cystic fibrosis using linked DNA markers and microvillar intestinal enzyme analysisJ E Spence, G J Buffone, C L Rosenbloom, et al.
Journal of Neurogenetics|December 1, 1985
Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophyL H Yamaoka, R J Bartlett, D A Ross, et al.
Prenatal Diagnosis|May 1, 1992
Cytogenetic results from the U.S. Collaborative Study on CVSD H Ledbetter, J M Zachary, J L Simpson, et al.
American Journal of Human Genetics|February 1, 1988
Uniparental disomy as a mechanism for human genetic diseaseJ E Spence, R G Perciaccante, G M Greig, et al.
Genomics|May 23, 1998
The human ROX gene: genomic structure and mutation analysis in human breast tumorsC Lo Nigro, T Venesio, A Reymond, et al.
Clinical Genetics|June 14, 2000
Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15W P Robinson, S L Christian, B D Kuchinka, et al.
Pageof 39