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E Frengen

Showing results (11-20 of 26) with videos related to

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Gene|July 31, 2012
1.5Mb deletion of chromosome 4p16.3 associated with postnatal growth delay, psychomotor impairment, epilepsy, impulsive behavior and asynchronous skeletal developmentD Misceo, T Barøy, J R Helle, et al.
Genetic Analysis : Biomolecular Engineering|December 28, 1999
The gene for human transcription factor TCF11 is located telomeric to D17S1827, BTR and HP1Hsbeta on chromosome 17q22N Skammelsrud, E R Martin, P Murphy, et al.
Hereditas|January 1, 1990
Isolation, characterization and chromosomal assignment of a partial cDNA for porcine 6-phosphogluconate dehydrogenaseI Harbitz, B Chowdhary, R Chowdhary, et al.
European Journal of Biochemistry|October 9, 2001
Identification of novel splice variants of the human catalytic subunit Cbeta of cAMP-dependent protein kinaseS Ørstavik, N Reinton, E Frengen, et al.
Genomics|June 22, 1999
A modular, positive selection bacterial artificial chromosome vector with multiple cloning sitesE Frengen, D Weichenhan, B Zhao, et al.
Gene|October 8, 2013
Post-zygotic breakage of a dicentric chromosome results in mosaicism for a telocentric 9p marker chromosome in a boy with developmental delayC R J Pedurupillay, D Misceo, T H Gamage, et al.
Cytogenetics and Cell Genetics|January 1, 1997
The gene cluster containing the LCAT gene is conserved between human and pigE Frengen, P D Thomsen, G Brede, et al.
Gene|February 11, 2014
A de novo 2.3 Mb deletion in 2q24.2q24.3 in a 20-month-old developmentally delayed girlV Belengeanu, T H Gamage, S Farcas, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan-McDermid syndrome and hypergonadotropic hypogonadismD Misceo, O K Rødningen, T Barøy, et al.
Genomics|September 19, 1998
An improved approach for construction of bacterial artificial chromosome librariesK Osoegawa, P Y Woon, B Zhao, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Gene|July 31, 2012
1.5Mb deletion of chromosome 4p16.3 associated with postnatal growth delay, psychomotor impairment, epilepsy, impulsive behavior and asynchronous skeletal developmentD Misceo, T Barøy, J R Helle, et al.
Genetic Analysis : Biomolecular Engineering|December 28, 1999
The gene for human transcription factor TCF11 is located telomeric to D17S1827, BTR and HP1Hsbeta on chromosome 17q22N Skammelsrud, E R Martin, P Murphy, et al.
Hereditas|January 1, 1990
Isolation, characterization and chromosomal assignment of a partial cDNA for porcine 6-phosphogluconate dehydrogenaseI Harbitz, B Chowdhary, R Chowdhary, et al.
European Journal of Biochemistry|October 9, 2001
Identification of novel splice variants of the human catalytic subunit Cbeta of cAMP-dependent protein kinaseS Ørstavik, N Reinton, E Frengen, et al.
Genomics|June 22, 1999
A modular, positive selection bacterial artificial chromosome vector with multiple cloning sitesE Frengen, D Weichenhan, B Zhao, et al.
Gene|October 8, 2013
Post-zygotic breakage of a dicentric chromosome results in mosaicism for a telocentric 9p marker chromosome in a boy with developmental delayC R J Pedurupillay, D Misceo, T H Gamage, et al.
Cytogenetics and Cell Genetics|January 1, 1997
The gene cluster containing the LCAT gene is conserved between human and pigE Frengen, P D Thomsen, G Brede, et al.
Gene|February 11, 2014
A de novo 2.3 Mb deletion in 2q24.2q24.3 in a 20-month-old developmentally delayed girlV Belengeanu, T H Gamage, S Farcas, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan-McDermid syndrome and hypergonadotropic hypogonadismD Misceo, O K Rødningen, T Barøy, et al.
Genomics|September 19, 1998
An improved approach for construction of bacterial artificial chromosome librariesK Osoegawa, P Y Woon, B Zhao, et al.
Pageof 3