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R Fitzpatrick

Showing results (441-450 of 555) with videos related to

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Human Molecular Genetics|December 9, 2010
Esrrg functions in early branch generation of the ureteric bud and is essential for normal development of the renal papillaRachel Berry, Louise Harewood, Liming Pei, et al.
Nature|October 1, 2020
A single bacterial genus maintains root growth in a complex microbiomeOmri M Finkel, Isai Salas-González, Gabriel Castrillo, et al.
American Journal of Medical Genetics. Part A|November 13, 2007
Beckwith-Wiedemann-like macroglossia and 18q23 haploinsufficiencyFrédéric Lirussi, Laurence Jonard, Véronique Gaston, et al.
Nature Genetics|March 4, 2003
Mutations in SOX2 cause anophthalmiaJudy Fantes, Nicola K Ragge, Sally-Ann Lynch, et al.
European Journal of Medical Genetics|December 5, 2016
Clinical features associated with CTNNB1 de novo loss of function mutations in ten individualsMira Kharbanda, Daniela T Pilz, Susan Tomkins, et al.
Human Molecular Genetics|August 14, 2003
Identification of SATB2 as the cleft palate gene on 2q32-q33David R FitzPatrick, Ian M Carr, Lorna McLaren, et al.
Science (New York, N.Y.)|September 6, 2008
Human-specific gain of function in a developmental enhancerShyam Prabhakar, Axel Visel, Jennifer A Akiyama, et al.
Epilepsia|March 15, 2006
Role of SOX2 mutations in human hippocampal malformations and epilepsySanjay M Sisodiya, Nicola K Ragge, Gianpiero L Cavalleri, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
Definition of 5q11.2 microdeletion syndrome reveals overlap with CHARGE syndrome and 22q11 deletion syndrome phenotypesCharlotte Snijders Blok, Nicole Corsten-Janssen, David R FitzPatrick, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Recurrence of SOX2 anophthalmia syndrome with gonosomal mosaicism in a phenotypically normal motherLaurence Faivre, Kathleen A Williamson, Valérie Faber, et al.
Pageof 56

Showing results (441-450 of 555) with videos related to

Sort By:
Pageof 56
Human Molecular Genetics|December 9, 2010
Esrrg functions in early branch generation of the ureteric bud and is essential for normal development of the renal papillaRachel Berry, Louise Harewood, Liming Pei, et al.
Nature|October 1, 2020
A single bacterial genus maintains root growth in a complex microbiomeOmri M Finkel, Isai Salas-González, Gabriel Castrillo, et al.
American Journal of Medical Genetics. Part A|November 13, 2007
Beckwith-Wiedemann-like macroglossia and 18q23 haploinsufficiencyFrédéric Lirussi, Laurence Jonard, Véronique Gaston, et al.
Nature Genetics|March 4, 2003
Mutations in SOX2 cause anophthalmiaJudy Fantes, Nicola K Ragge, Sally-Ann Lynch, et al.
European Journal of Medical Genetics|December 5, 2016
Clinical features associated with CTNNB1 de novo loss of function mutations in ten individualsMira Kharbanda, Daniela T Pilz, Susan Tomkins, et al.
Human Molecular Genetics|August 14, 2003
Identification of SATB2 as the cleft palate gene on 2q32-q33David R FitzPatrick, Ian M Carr, Lorna McLaren, et al.
Science (New York, N.Y.)|September 6, 2008
Human-specific gain of function in a developmental enhancerShyam Prabhakar, Axel Visel, Jennifer A Akiyama, et al.
Epilepsia|March 15, 2006
Role of SOX2 mutations in human hippocampal malformations and epilepsySanjay M Sisodiya, Nicola K Ragge, Gianpiero L Cavalleri, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
Definition of 5q11.2 microdeletion syndrome reveals overlap with CHARGE syndrome and 22q11 deletion syndrome phenotypesCharlotte Snijders Blok, Nicole Corsten-Janssen, David R FitzPatrick, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Recurrence of SOX2 anophthalmia syndrome with gonosomal mosaicism in a phenotypically normal motherLaurence Faivre, Kathleen A Williamson, Valérie Faber, et al.
Pageof 56