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R Fitzpatrick

Showing results (491-500 of 555) with videos related to

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Plos Genetics|December 6, 2005
Medical sequencing of candidate genes for nonsyndromic cleft lip and palateAlexandre R Vieira, Joseph R Avila, Sandra Daack-Hirsch, et al.
American Journal of Human Genetics|May 27, 2005
3q29 microdeletion syndrome: clinical and molecular characterization of a new syndromeLionel Willatt, James Cox, John Barber, et al.
Nature Communications|October 13, 2019
Contribution of retrotransposition to developmental disordersEugene J Gardner, Elena Prigmore, Giuseppe Gallone, et al.
Nature Communications|January 28, 2021
The contribution of X-linked coding variation to severe developmental disordersHilary C Martin, Eugene J Gardner, Kaitlin E Samocha, et al.
Immunity|December 1, 2001
A critical role for Dnmt1 and DNA methylation in T cell development, function, and survivalP P Lee, D R Fitzpatrick, C Beard, et al.
Nature Genetics|May 10, 2011
Mutations in CEP57 cause mosaic variegated aneuploidy syndromeKatie Snape, Sandra Hanks, Elise Ruark, et al.
Science (New York, N.Y.)|October 26, 2013
Fine tuning of craniofacial morphology by distant-acting enhancersCatia Attanasio, Alex S Nord, Yiwen Zhu, et al.
Plos Genetics|March 12, 2019
ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathyMark T Handley, Kaalak Reddy, Jimi Wills, et al.
General and Comparative Endocrinology|May 8, 2018
Gene transcription ontogeny of hypothalamic-pituitary-thyroid axis development in early-life stage fathead minnow and zebrafishLucia Vergauwen, Jenna E Cavallin, Gerald T Ankley, et al.
Human Molecular Genetics|June 14, 2012
Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODHJoe Rainger, Hemant Bengani, Leigh Campbell, et al.
Pageof 56

Showing results (491-500 of 555) with videos related to

Sort By:
Pageof 56
Plos Genetics|December 6, 2005
Medical sequencing of candidate genes for nonsyndromic cleft lip and palateAlexandre R Vieira, Joseph R Avila, Sandra Daack-Hirsch, et al.
American Journal of Human Genetics|May 27, 2005
3q29 microdeletion syndrome: clinical and molecular characterization of a new syndromeLionel Willatt, James Cox, John Barber, et al.
Nature Communications|October 13, 2019
Contribution of retrotransposition to developmental disordersEugene J Gardner, Elena Prigmore, Giuseppe Gallone, et al.
Nature Communications|January 28, 2021
The contribution of X-linked coding variation to severe developmental disordersHilary C Martin, Eugene J Gardner, Kaitlin E Samocha, et al.
Immunity|December 1, 2001
A critical role for Dnmt1 and DNA methylation in T cell development, function, and survivalP P Lee, D R Fitzpatrick, C Beard, et al.
Nature Genetics|May 10, 2011
Mutations in CEP57 cause mosaic variegated aneuploidy syndromeKatie Snape, Sandra Hanks, Elise Ruark, et al.
Science (New York, N.Y.)|October 26, 2013
Fine tuning of craniofacial morphology by distant-acting enhancersCatia Attanasio, Alex S Nord, Yiwen Zhu, et al.
Plos Genetics|March 12, 2019
ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathyMark T Handley, Kaalak Reddy, Jimi Wills, et al.
General and Comparative Endocrinology|May 8, 2018
Gene transcription ontogeny of hypothalamic-pituitary-thyroid axis development in early-life stage fathead minnow and zebrafishLucia Vergauwen, Jenna E Cavallin, Gerald T Ankley, et al.
Human Molecular Genetics|June 14, 2012
Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODHJoe Rainger, Hemant Bengani, Leigh Campbell, et al.
Pageof 56