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C A Walsh

Showing results (91-100 of 128) with videos related to

Pageof 13
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Neurology|August 3, 1999
Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephalyW B Dobyns, C L Truwit, M E Ross, et al.
Pediatric Radiology|December 2, 2000
Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findingsT Y Poussaint, J W Fox, W B Dobyns, et al.
Physical Review Letters|October 16, 2020
Magnetic Signatures of Radiation-Driven Double Ablation FrontsP T Campbell, C A Walsh, B K Russell, et al.
Journal of Medical Genetics|June 3, 2004
Broader geographical spectrum of Cohen syndrome due to COH1 mutationsG H Mochida, A Rajab, W Eyaid, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|May 31, 2014
Mode of delivery in pregnancies complicated by major fetal congenital heart disease: a retrospective cohort studyC A Walsh, A MacTiernan, S Farrell, et al.
Neurology|March 26, 2003
Periventricular heterotopia associated with chromosome 5p anomaliesV L Sheen, J W Wheless, A Bodell, et al.
Neurology|December 7, 2007
A structural basis for reading fluency: white matter defects in a genetic brain malformationB S Chang, T Katzir, T Liu, et al.
Neuron|August 1, 1997
Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouseM L Ware, J W Fox, J L González, et al.
The American Journal of Psychiatry|November 3, 2001
Childhood abuse and lifetime psychopathology in a community sampleH L MacMillan, J E Fleming, D L Streiner, et al.
Neurology|April 12, 2003
Autosomal recessive form of periventricular heterotopiaV L Sheen, M Topçu, S Berkovic, et al.
Pageof 13

Showing results (91-100 of 128) with videos related to

Sort By:
Pageof 13
Neurology|August 3, 1999
Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephalyW B Dobyns, C L Truwit, M E Ross, et al.
Pediatric Radiology|December 2, 2000
Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findingsT Y Poussaint, J W Fox, W B Dobyns, et al.
Physical Review Letters|October 16, 2020
Magnetic Signatures of Radiation-Driven Double Ablation FrontsP T Campbell, C A Walsh, B K Russell, et al.
Journal of Medical Genetics|June 3, 2004
Broader geographical spectrum of Cohen syndrome due to COH1 mutationsG H Mochida, A Rajab, W Eyaid, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|May 31, 2014
Mode of delivery in pregnancies complicated by major fetal congenital heart disease: a retrospective cohort studyC A Walsh, A MacTiernan, S Farrell, et al.
Neurology|March 26, 2003
Periventricular heterotopia associated with chromosome 5p anomaliesV L Sheen, J W Wheless, A Bodell, et al.
Neurology|December 7, 2007
A structural basis for reading fluency: white matter defects in a genetic brain malformationB S Chang, T Katzir, T Liu, et al.
Neuron|August 1, 1997
Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouseM L Ware, J W Fox, J L González, et al.
The American Journal of Psychiatry|November 3, 2001
Childhood abuse and lifetime psychopathology in a community sampleH L MacMillan, J E Fleming, D L Streiner, et al.
Neurology|April 12, 2003
Autosomal recessive form of periventricular heterotopiaV L Sheen, M Topçu, S Berkovic, et al.
Pageof 13