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M Leppert

Showing results (31-40 of 315) with videos related to

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Journal of Neonatal-Perinatal Medicine|October 21, 2015
Test-retest reliability of the Capute scales for neurodevelopmental screening of a high risk sample: Impact of test-retest interval and degree of neonatal riskM McCurdy, A Bellows, D Deng, et al.
Human Molecular Genetics|September 1, 1994
SSC polymorphisms in interleukin genesL Borish, J J Mascali, M Klinnert, et al.
Neurology|February 1, 1992
Linkage of atypical myotonia congenita to a sodium channel locusL J Ptacek, R Tawil, R C Griggs, et al.
Genomics|June 1, 1990
Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1qR A Lewis, B Otterud, D Stauffer, et al.
Human Genetics|January 1, 1986
Tetraploid partial hydatidiform moles: two cases with a triple paternal contribution and a 92,XXXY karyotypeU Surti, A E Szulman, K Wagner, et al.
American Journal of Human Genetics|August 1, 1991
Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locusL J Ptacek, F Tyler, J S Trimmer, et al.
Genomics|July 1, 1988
A primary map of ten DNA markers and two serological markers for human chromosome 19Y Nakamura, M Lathrop, P O'Connell, et al.
Neurology|July 1, 1993
Seizure characteristics in chromosome 20 benign familial neonatal convulsionsG M Ronen, T O Rosales, M Connolly, et al.
Cold Spring Harbor Symposia on Quantitative Biology|September 2, 2004
A model system for identifying genes underlying complex traitsD Drayna, U K Kim, H Coon, et al.
Science (New York, N.Y.)|May 3, 1991
Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 geneM Keating, D Atkinson, C Dunn, et al.
Pageof 32

Showing results (31-40 of 315) with videos related to

Sort By:
Pageof 32
Journal of Neonatal-Perinatal Medicine|October 21, 2015
Test-retest reliability of the Capute scales for neurodevelopmental screening of a high risk sample: Impact of test-retest interval and degree of neonatal riskM McCurdy, A Bellows, D Deng, et al.
Human Molecular Genetics|September 1, 1994
SSC polymorphisms in interleukin genesL Borish, J J Mascali, M Klinnert, et al.
Neurology|February 1, 1992
Linkage of atypical myotonia congenita to a sodium channel locusL J Ptacek, R Tawil, R C Griggs, et al.
Genomics|June 1, 1990
Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1qR A Lewis, B Otterud, D Stauffer, et al.
Human Genetics|January 1, 1986
Tetraploid partial hydatidiform moles: two cases with a triple paternal contribution and a 92,XXXY karyotypeU Surti, A E Szulman, K Wagner, et al.
American Journal of Human Genetics|August 1, 1991
Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locusL J Ptacek, F Tyler, J S Trimmer, et al.
Genomics|July 1, 1988
A primary map of ten DNA markers and two serological markers for human chromosome 19Y Nakamura, M Lathrop, P O'Connell, et al.
Neurology|July 1, 1993
Seizure characteristics in chromosome 20 benign familial neonatal convulsionsG M Ronen, T O Rosales, M Connolly, et al.
Cold Spring Harbor Symposia on Quantitative Biology|September 2, 2004
A model system for identifying genes underlying complex traitsD Drayna, U K Kim, H Coon, et al.
Science (New York, N.Y.)|May 3, 1991
Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 geneM Keating, D Atkinson, C Dunn, et al.
Pageof 32