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L G Biesecker

Showing results (71-80 of 89) with videos related to

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Journal of Medical Genetics|June 1, 1997
Linkage mapping and phenotypic analysis of autosomal dominant Pallister-Hall syndromeS Kang, J Allen, J M Graham, et al.
American Journal of Human Genetics|May 1, 1993
Molecular analysis of the 18q- syndrome--and correlation with phenotypeA D Kline, M E White, R Wapner, et al.
American Journal of Human Genetics|August 23, 2000
A novel nemaline myopathy in the Amish caused by a mutation in troponin T1J J Johnston, R I Kelley, T O Crawford, et al.
Journal of Medical Genetics|November 1, 1996
Exclusion of candidate loci and cholesterol biosynthetic abnormalities in familial Pallister-Hall syndromeL G Biesecker, S Kang, A A Schäffer, et al.
Clinical Genetics|December 8, 2016
PUGS: A novel scale to assess perceptions of uncertainties in genome sequencingB B Biesecker, S W Woolford, W M P Klein, et al.
Clinical Genetics|April 15, 2018
Correction to: PUGS: A novel scale to assess perceptions of uncertainties in genome sequencingB B Biesecker, S W Woolford, W M P Klein, et al.
Genomics|August 1, 1992
Identification of new markers in Xp21 between DXS28 (C7) and DMDK C Worley, J A Towbin, X M Zhu, et al.
Clinical Genetics|May 13, 2014
Determination of the allelic frequency in Smith-Lemli-Opitz syndrome by analysis of massively parallel sequencing data setsJ L Cross, J Iben, C L Simpson, et al.
Genome Research|October 6, 1997
Characterization of short tandem repeats from thirty-one human telomeresM Rosenberg, L Hui, J Ma, et al.
Nature Genetics|September 6, 2000
Mutations in MKKS cause Bardet-Biedl syndromeA M Slavotinek, E M Stone, K Mykytyn, et al.
Pageof 9

Showing results (71-80 of 89) with videos related to

Sort By:
Pageof 9
Journal of Medical Genetics|June 1, 1997
Linkage mapping and phenotypic analysis of autosomal dominant Pallister-Hall syndromeS Kang, J Allen, J M Graham, et al.
American Journal of Human Genetics|May 1, 1993
Molecular analysis of the 18q- syndrome--and correlation with phenotypeA D Kline, M E White, R Wapner, et al.
American Journal of Human Genetics|August 23, 2000
A novel nemaline myopathy in the Amish caused by a mutation in troponin T1J J Johnston, R I Kelley, T O Crawford, et al.
Journal of Medical Genetics|November 1, 1996
Exclusion of candidate loci and cholesterol biosynthetic abnormalities in familial Pallister-Hall syndromeL G Biesecker, S Kang, A A Schäffer, et al.
Clinical Genetics|December 8, 2016
PUGS: A novel scale to assess perceptions of uncertainties in genome sequencingB B Biesecker, S W Woolford, W M P Klein, et al.
Clinical Genetics|April 15, 2018
Correction to: PUGS: A novel scale to assess perceptions of uncertainties in genome sequencingB B Biesecker, S W Woolford, W M P Klein, et al.
Genomics|August 1, 1992
Identification of new markers in Xp21 between DXS28 (C7) and DMDK C Worley, J A Towbin, X M Zhu, et al.
Clinical Genetics|May 13, 2014
Determination of the allelic frequency in Smith-Lemli-Opitz syndrome by analysis of massively parallel sequencing data setsJ L Cross, J Iben, C L Simpson, et al.
Genome Research|October 6, 1997
Characterization of short tandem repeats from thirty-one human telomeresM Rosenberg, L Hui, J Ma, et al.
Nature Genetics|September 6, 2000
Mutations in MKKS cause Bardet-Biedl syndromeA M Slavotinek, E M Stone, K Mykytyn, et al.
Pageof 9