Frank J Probst - JoVE Visualize

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Methods in Enzymology|August 12, 2010

Mouse mutagenesis with the chemical supermutagen ENUFrank J Probst, Monica J Justice

The Journal of Heredity|May 24, 2008

Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner SyndromeFrank J Probst, Mitchell Lance Cooper, Sau Wai Cheung, et al.

European Journal of Pediatrics|November 13, 2014

Syngnathia and obstructive apnea in a case of popliteal pterygium syndromeJennifer E Posey, Vedanta Dariya, Joseph L Edmonds, et al.

Hearing Research|April 4, 2006

Transgene correction maintains normal cochlear structure and function in 6-month-old Myo15a mutant miceSho Kanzaki, Lisa Beyer, I Jill Karolyi, et al.

American Journal of Medical Genetics|July 19, 2002

Exclusion of PITX2 mutations as a major cause of CHARGE associationDonna M Martin, Frank J Probst, Sharon E Fox, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 28, 2007

Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid miceI Jill Karolyi, Gary A Dootz, Karin Halsey, et al.

Plos One|December 5, 2013

A point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus)Frank J Probst, Rebecca R Corrigan, Daniela Del Gaudio, et al.

Human Molecular Genetics|September 11, 2003

Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereociliaI Jill Karolyi, Frank J Probst, Lisa Beyer, et al.

Scientific Reports|May 29, 2021

Transcriptome analysis of MBD5-associated neurodevelopmental disorder (MAND) neural progenitor cells reveals dysregulation of autism-associated genesSureni V Mullegama, Steven D Klein, Stephen R Williams, et al.

Journal of Medical Genetics|October 9, 2012

Co-occurrence of recurrent duplications of the DiGeorge syndrome region on both chromosome 22 homologues due to inherited and de novo eventsWeimin Bi, Frank J Probst, Joanna Wiszniewska, et al.

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Showing results (1-10 of 24) with videos related to

Sort By:

Pageof 3

Methods in Enzymology|August 12, 2010

Mouse mutagenesis with the chemical supermutagen ENUFrank J Probst, Monica J Justice

The Journal of Heredity|May 24, 2008

Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner SyndromeFrank J Probst, Mitchell Lance Cooper, Sau Wai Cheung, et al.

European Journal of Pediatrics|November 13, 2014

Syngnathia and obstructive apnea in a case of popliteal pterygium syndromeJennifer E Posey, Vedanta Dariya, Joseph L Edmonds, et al.

Hearing Research|April 4, 2006

Transgene correction maintains normal cochlear structure and function in 6-month-old Myo15a mutant miceSho Kanzaki, Lisa Beyer, I Jill Karolyi, et al.

American Journal of Medical Genetics|July 19, 2002

Exclusion of PITX2 mutations as a major cause of CHARGE associationDonna M Martin, Frank J Probst, Sharon E Fox, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 28, 2007

Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid miceI Jill Karolyi, Gary A Dootz, Karin Halsey, et al.

Plos One|December 5, 2013

A point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus)Frank J Probst, Rebecca R Corrigan, Daniela Del Gaudio, et al.

Human Molecular Genetics|September 11, 2003

Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereociliaI Jill Karolyi, Frank J Probst, Lisa Beyer, et al.

Scientific Reports|May 29, 2021

Transcriptome analysis of MBD5-associated neurodevelopmental disorder (MAND) neural progenitor cells reveals dysregulation of autism-associated genesSureni V Mullegama, Steven D Klein, Stephen R Williams, et al.

Journal of Medical Genetics|October 9, 2012

Co-occurrence of recurrent duplications of the DiGeorge syndrome region on both chromosome 22 homologues due to inherited and de novo eventsWeimin Bi, Frank J Probst, Joanna Wiszniewska, et al.

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