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David R FitzPatrick

Showing results (51-60 of 144) with videos related to

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Nature|March 22, 2018
De novo mutations in regulatory elements in neurodevelopmental disordersPatrick J Short, Jeremy F McRae, Giuseppe Gallone, et al.
Nature Communications|April 26, 2024
Single-cell analyses reveal transient retinal progenitor cells in the ciliary margin of developing human retinaBirthe Dorgau, Joseph Collin, Agata Rozanska, et al.
European Journal of Immunology|October 16, 2004
Paradoxical role of programmed death-1 ligand 2 in Th2 immune responses in vitro and in a mouse asthma model in vivoEzogelin Oflazoglu, David A Swart, Penny Anders-Bartholo, et al.
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.
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.
Pageof 15

Showing results (51-60 of 144) with videos related to

Sort By:
Pageof 15
Nature|March 22, 2018
De novo mutations in regulatory elements in neurodevelopmental disordersPatrick J Short, Jeremy F McRae, Giuseppe Gallone, et al.
Nature Communications|April 26, 2024
Single-cell analyses reveal transient retinal progenitor cells in the ciliary margin of developing human retinaBirthe Dorgau, Joseph Collin, Agata Rozanska, et al.
European Journal of Immunology|October 16, 2004
Paradoxical role of programmed death-1 ligand 2 in Th2 immune responses in vitro and in a mouse asthma model in vivoEzogelin Oflazoglu, David A Swart, Penny Anders-Bartholo, et al.
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.
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.
Pageof 15