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D H Ledbetter

Showing results (151-160 of 251) with videos related to

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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.
Prenatal Diagnosis|September 1, 1996
Cytogenetic and age-dependent risk factors associated with uniparental disomy 15W P Robinson, S Langlois, S Schuffenhauer, et al.
American Journal of Medical Genetics|July 9, 1999
Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3T I Pollin, W B Dobyns, C A Crowe, et al.
American Journal of Human Genetics|November 1, 1988
Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndromeP vanTuinen, W B Dobyns, D C Rich, et al.
Pageof 26

Showing results (151-160 of 251) with videos related to

Sort By:
Pageof 26
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.
Prenatal Diagnosis|September 1, 1996
Cytogenetic and age-dependent risk factors associated with uniparental disomy 15W P Robinson, S Langlois, S Schuffenhauer, et al.
American Journal of Medical Genetics|July 9, 1999
Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3T I Pollin, W B Dobyns, C A Crowe, et al.
American Journal of Human Genetics|November 1, 1988
Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndromeP vanTuinen, W B Dobyns, D C Rich, et al.
Pageof 26