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Altherr

Showing results (41-50 of 127) with videos related to

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Neurology|November 1, 1993
Genetics of facioscapulohumeral muscular dystrophy: new mutations in sporadic casesR C Griggs, R Tawil, D Storvick, et al.
American Journal of Medical Genetics|June 19, 1995
Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: construction of a laser microdissection libraryM Upadhyaya, M Osborn, J Maynard, et al.
Human Molecular Genetics|March 1, 1997
The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD regionS T Winokur, U Bengtsson, J C Vargas, et al.
International Psychogeriatrics|November 18, 2016
Relocation experiences with unplanned admission to a nursing home: a qualitative studyAndrea Luise Koppitz, Jutta Dreizler, Jeanine Altherr, et al.
International Journal of Exercise Science|September 27, 2021
The Influence of a Total Body Resistance Training Program on Autonomic Modulation and Strength Variables in Young AdultsCody A Altherr, Kayla M Soave, Paul R Nagelkirk, et al.
Genomics|October 1, 1989
Isolation of a novel mildly repetitive DNA sequence that is predominantly located at the terminus of the short arm of chromosome 4 near the Huntington disease geneM R Altherr, B Smith, M E MacDonald, et al.
Journal of Medical Genetics|January 1, 1995
A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)patW el-Rifai, J Leisti, M Kähkönen, et al.
The Journal of Cell Biology|October 23, 1997
Actinin-associated LIM protein: identification of a domain interaction between PDZ and spectrin-like repeat motifsH Xia, S T Winokur, W L Kuo, et al.
American Journal of Medical Genetics|July 11, 1997
Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairsM R Altherr, T J Wright, K Denison, et al.
Genomics|April 1, 1994
Chromosomal localization of the gonadotropin-releasing hormone receptor gene to human chromosome 4q13.1-q21.1 and mouse chromosome 5U B Kaiser, H Dushkin, M R Altherr, et al.
Pageof 13

Showing results (41-50 of 127) with videos related to

Sort By:
Pageof 13
Neurology|November 1, 1993
Genetics of facioscapulohumeral muscular dystrophy: new mutations in sporadic casesR C Griggs, R Tawil, D Storvick, et al.
American Journal of Medical Genetics|June 19, 1995
Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: construction of a laser microdissection libraryM Upadhyaya, M Osborn, J Maynard, et al.
Human Molecular Genetics|March 1, 1997
The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD regionS T Winokur, U Bengtsson, J C Vargas, et al.
International Psychogeriatrics|November 18, 2016
Relocation experiences with unplanned admission to a nursing home: a qualitative studyAndrea Luise Koppitz, Jutta Dreizler, Jeanine Altherr, et al.
International Journal of Exercise Science|September 27, 2021
The Influence of a Total Body Resistance Training Program on Autonomic Modulation and Strength Variables in Young AdultsCody A Altherr, Kayla M Soave, Paul R Nagelkirk, et al.
Genomics|October 1, 1989
Isolation of a novel mildly repetitive DNA sequence that is predominantly located at the terminus of the short arm of chromosome 4 near the Huntington disease geneM R Altherr, B Smith, M E MacDonald, et al.
Journal of Medical Genetics|January 1, 1995
A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)patW el-Rifai, J Leisti, M Kähkönen, et al.
The Journal of Cell Biology|October 23, 1997
Actinin-associated LIM protein: identification of a domain interaction between PDZ and spectrin-like repeat motifsH Xia, S T Winokur, W L Kuo, et al.
American Journal of Medical Genetics|July 11, 1997
Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairsM R Altherr, T J Wright, K Denison, et al.
Genomics|April 1, 1994
Chromosomal localization of the gonadotropin-releasing hormone receptor gene to human chromosome 4q13.1-q21.1 and mouse chromosome 5U B Kaiser, H Dushkin, M R Altherr, et al.
Pageof 13