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Clinical Genetics
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July 12, 2008
Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4
E Steichen-Gersdorf, I Gassner, A Superti-Furga, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
August 25, 2005
The Air noncoding RNA: an imprinted cis-silencing transcript
G Braidotti, T Baubec, F Pauler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 19, 2009
A variable neurodegenerative phenotype with polymerase gamma mutation
S Stricker, H Prüss, R Horvath, et al.
Developmental and Comparative Immunology
|
June 12, 2003
A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolution
S Stricker, A J Poustka, U Wiecha, et al.
NPJ Parkinson'S Disease
|
September 16, 2022
Parkinson-causing mutations in LRRK2 impair the physiological tetramerization of endogenous α-synuclein in human neurons
Luis Fonseca-Ornelas, Jonathan M S Stricker, Stephanie Soriano-Cruz, et al.
Gene Expression Patterns : GEP
|
July 11, 2006
Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2(-/-) mouse model
J Hecht, V Seitz, M Urban, et al.
AJNR. American Journal of Neuroradiology
|
October 30, 2020
Risk Factors for Early Brain AVM Rupture: Cohort Study of Pediatric and Adult Patients
L Garzelli, E Shotar, T Blauwblomme, et al.
AJNR. American Journal of Neuroradiology
|
August 25, 2022
Noninvasive Follow-up Imaging of Ruptured Pediatric Brain AVMs Using Arterial Spin-Labeling
J F Hak, G Boulouis, B Kerleroux, et al.
Nature Communications
|
November 21, 2023
Small molecule regulators of microRNAs identified by high-throughput screen coupled with high-throughput sequencing
Lien D Nguyen, Zhiyun Wei, M Catarina Silva, et al.
American Journal of Human Genetics
|
July 11, 2006
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome
C G Woods, S Stricker, P Seemann, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Clinical Genetics
|
July 12, 2008
Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4
E Steichen-Gersdorf, I Gassner, A Superti-Furga, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
August 25, 2005
The Air noncoding RNA: an imprinted cis-silencing transcript
G Braidotti, T Baubec, F Pauler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 19, 2009
A variable neurodegenerative phenotype with polymerase gamma mutation
S Stricker, H Prüss, R Horvath, et al.
Developmental and Comparative Immunology
|
June 12, 2003
A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolution
S Stricker, A J Poustka, U Wiecha, et al.
NPJ Parkinson'S Disease
|
September 16, 2022
Parkinson-causing mutations in LRRK2 impair the physiological tetramerization of endogenous α-synuclein in human neurons
Luis Fonseca-Ornelas, Jonathan M S Stricker, Stephanie Soriano-Cruz, et al.
Gene Expression Patterns : GEP
|
July 11, 2006
Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2(-/-) mouse model
J Hecht, V Seitz, M Urban, et al.
AJNR. American Journal of Neuroradiology
|
October 30, 2020
Risk Factors for Early Brain AVM Rupture: Cohort Study of Pediatric and Adult Patients
L Garzelli, E Shotar, T Blauwblomme, et al.
AJNR. American Journal of Neuroradiology
|
August 25, 2022
Noninvasive Follow-up Imaging of Ruptured Pediatric Brain AVMs Using Arterial Spin-Labeling
J F Hak, G Boulouis, B Kerleroux, et al.
Nature Communications
|
November 21, 2023
Small molecule regulators of microRNAs identified by high-throughput screen coupled with high-throughput sequencing
Lien D Nguyen, Zhiyun Wei, M Catarina Silva, et al.
American Journal of Human Genetics
|
July 11, 2006
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome
C G Woods, S Stricker, P Seemann, et al.
Page
of 3