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Stroke
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January 14, 2016
Cortical Sparing in Preterm Ischemic Arterial Stroke
Niek E van der Aa, Manon J N L Benders, Peter G Nikkels, et al.
American Journal of Medical Genetics. Part A
|
September 5, 2003
Prenatal diagnosis of boomerang dysplasia
Marja W Wessels, Nicolette S Den Hollander, Ronald R De Krijger, et al.
Pediatric Radiology
|
July 3, 2017
Apparent diffusion coefficient as it relates to histopathology findings in post-chemotherapy nephroblastoma: a feasibility study
Annemieke S Littooij, Peter G Nikkels, Christina A Hulsbergen-van de Kaa, et al.
Nature Medicine
|
October 24, 2007
Nucleotide-sugar transporter SLC35D1 is critical to chondroitin sulfate synthesis in cartilage and skeletal development in mouse and human
Shuichi Hiraoka, Tatsuya Furuichi, Gen Nishimura, et al.
American Journal of Human Genetics
|
October 25, 2011
Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid
Kathrin Laue, Hans-Martin Pogoda, Philip B Daniel, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Stroke
|
January 14, 2016
Cortical Sparing in Preterm Ischemic Arterial Stroke
Niek E van der Aa, Manon J N L Benders, Peter G Nikkels, et al.
American Journal of Medical Genetics. Part A
|
September 5, 2003
Prenatal diagnosis of boomerang dysplasia
Marja W Wessels, Nicolette S Den Hollander, Ronald R De Krijger, et al.
Pediatric Radiology
|
July 3, 2017
Apparent diffusion coefficient as it relates to histopathology findings in post-chemotherapy nephroblastoma: a feasibility study
Annemieke S Littooij, Peter G Nikkels, Christina A Hulsbergen-van de Kaa, et al.
Nature Medicine
|
October 24, 2007
Nucleotide-sugar transporter SLC35D1 is critical to chondroitin sulfate synthesis in cartilage and skeletal development in mouse and human
Shuichi Hiraoka, Tatsuya Furuichi, Gen Nishimura, et al.
American Journal of Human Genetics
|
October 25, 2011
Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid
Kathrin Laue, Hans-Martin Pogoda, Philip B Daniel, et al.
Page
of 1