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H R Slater

Showing results (21-30 of 38) with videos related to

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Scientific Reports|July 9, 2016
β-glucuronidase mRNA levels are correlated with gait and working memory in premutation females: understanding the role of FMR1 premutation allelesC M Kraan, K M Cornish, Q M Bui, et al.
Journal of Medical Genetics|May 5, 1999
Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissectionM B Delatycki, L Voullaire, D Francis, et al.
Journal of Medical Genetics|March 1, 1988
Interstitial deletion (6) (q11----q15) in an infant with congenital abnormalitiesH R Slater, A Robb, L A Forsyth, et al.
Journal of Medical Genetics|December 7, 2007
A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changesD Z Loesch, M Cook, L Litewka, et al.
Prenatal Diagnosis|July 27, 1999
Maternal uniparental isodisomy for chromosome 14 detected prenatallyA Ralph, F Scott, C Tiernan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 30, 2011
White matter changes in basis pontis in small expansion FMR1 allele carriers with parkinsonismD Z Loesch, K Kotschet, N Trost, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Superior verbal ability and nonverbal learning disability in a child with a novel 17p12p13.1 deletionD L Steele, A K Chisholm, J D R McGhie, et al.
Clinical Genetics|December 4, 2012
New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's diseaseD Z Loesch, F Tassone, J Lo, et al.
Cytogenetic and Genome Research|November 20, 2002
Identification of a haplosufficient 3.6-Mb region in human chromosome 11q14.3-->q21L Li, P Moore, C Ngo, et al.
Translational Psychiatry|December 14, 2016
Brain structure and intragenic DNA methylation are correlated, and predict executive dysfunction in fragile X premutation femalesA L Shelton, K M Cornish, S Kolbe, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Scientific Reports|July 9, 2016
β-glucuronidase mRNA levels are correlated with gait and working memory in premutation females: understanding the role of FMR1 premutation allelesC M Kraan, K M Cornish, Q M Bui, et al.
Journal of Medical Genetics|May 5, 1999
Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissectionM B Delatycki, L Voullaire, D Francis, et al.
Journal of Medical Genetics|March 1, 1988
Interstitial deletion (6) (q11----q15) in an infant with congenital abnormalitiesH R Slater, A Robb, L A Forsyth, et al.
Journal of Medical Genetics|December 7, 2007
A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changesD Z Loesch, M Cook, L Litewka, et al.
Prenatal Diagnosis|July 27, 1999
Maternal uniparental isodisomy for chromosome 14 detected prenatallyA Ralph, F Scott, C Tiernan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 30, 2011
White matter changes in basis pontis in small expansion FMR1 allele carriers with parkinsonismD Z Loesch, K Kotschet, N Trost, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Superior verbal ability and nonverbal learning disability in a child with a novel 17p12p13.1 deletionD L Steele, A K Chisholm, J D R McGhie, et al.
Clinical Genetics|December 4, 2012
New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's diseaseD Z Loesch, F Tassone, J Lo, et al.
Cytogenetic and Genome Research|November 20, 2002
Identification of a haplosufficient 3.6-Mb region in human chromosome 11q14.3-->q21L Li, P Moore, C Ngo, et al.
Translational Psychiatry|December 14, 2016
Brain structure and intragenic DNA methylation are correlated, and predict executive dysfunction in fragile X premutation femalesA L Shelton, K M Cornish, S Kolbe, et al.
Pageof 4