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H Ledbetter

Showing results (191-200 of 388) with videos related to

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Nucleic Acids Research|August 11, 1990
Dinucleotide repeat polymorphisms at the D17S250 and D17S261 lociJ L Weber, A E Kwitek, P E May, et al.
Nature Genetics|September 1, 1994
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control regionJ S Sutcliffe, M Nakao, S Christian, et al.
Blood|January 1, 1988
Alteration and abnormal expression of the c-myc oncogene in human multiple myelomaP Selvanayagam, M Blick, F Narni, et al.
American Journal of Medical Genetics|September 1, 1988
Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomalyF Greenberg, K B Courtney, R A Wessels, et al.
American Journal of Human Genetics|September 1, 1984
Human chromosomal assignments for 14 argininosuccinate synthetase pseudogenes: cloned DNAs as reagents for cytogenetic analysisT S Su, R L Nussbaum, S Airhart, et al.
Metabolic and Pediatric Ophthalmology|January 1, 1980
Genetic heterogeneity of aniridia: negative linkage dataH M Hittner, V M Riccardi, R E Ferrell, et al.
Human Genetics|October 1, 1990
Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reactionJ R Batanian, S A Ledbetter, R K Wolff, et al.
Nature|August 19, 1993
Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeatsO Reiner, R Carrozzo, Y Shen, et al.
Nucleic Acids Research|February 25, 1990
Isolation of a polymorphic DNA sequence (LL101) from the short arm of chromosome 17 [D17S251]P I Patel, D H Ledbetter, S Frances, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 7, 2023
Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndromeCora M Taylor, Brenda M Finucane, Andres Moreno-De-Luca, et al.
Pageof 39

Showing results (191-200 of 388) with videos related to

Sort By:
Pageof 39
Nucleic Acids Research|August 11, 1990
Dinucleotide repeat polymorphisms at the D17S250 and D17S261 lociJ L Weber, A E Kwitek, P E May, et al.
Nature Genetics|September 1, 1994
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control regionJ S Sutcliffe, M Nakao, S Christian, et al.
Blood|January 1, 1988
Alteration and abnormal expression of the c-myc oncogene in human multiple myelomaP Selvanayagam, M Blick, F Narni, et al.
American Journal of Medical Genetics|September 1, 1988
Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomalyF Greenberg, K B Courtney, R A Wessels, et al.
American Journal of Human Genetics|September 1, 1984
Human chromosomal assignments for 14 argininosuccinate synthetase pseudogenes: cloned DNAs as reagents for cytogenetic analysisT S Su, R L Nussbaum, S Airhart, et al.
Metabolic and Pediatric Ophthalmology|January 1, 1980
Genetic heterogeneity of aniridia: negative linkage dataH M Hittner, V M Riccardi, R E Ferrell, et al.
Human Genetics|October 1, 1990
Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reactionJ R Batanian, S A Ledbetter, R K Wolff, et al.
Nature|August 19, 1993
Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeatsO Reiner, R Carrozzo, Y Shen, et al.
Nucleic Acids Research|February 25, 1990
Isolation of a polymorphic DNA sequence (LL101) from the short arm of chromosome 17 [D17S251]P I Patel, D H Ledbetter, S Frances, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 7, 2023
Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndromeCora M Taylor, Brenda M Finucane, Andres Moreno-De-Luca, et al.
Pageof 39